SHMARQL

disorder of vitamin and non-protein cofactor absorption and transport

<http://www.wikidata.org/entity/Q55787334>

human disease
rdfs:label
"disorder of vitamin and non-protein cofactor absorption and transport"@en
skos:altLabel "Disorder of vitamin and non-protein cofactor absorption and transport"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-24T00:03:05+00:00"^^xsd:dateTime
schema:version 2560161997
wikibase:identifiers 6
wikibase:sitelinks 0
wikibase:statements 38
p:P14914 wd:statement/Q55787334-87B13E24-5A44-490E-89AD-035942FD7B5C
p:P1550 wd:statement/Q55787334-981FCAF2-DF9E-48DC-A2EC-FD3057F9831C
p:P2293 wd:statement/Q55787334-00DD1BD8-1A86-4887-B364-744D1D7A596F
wd:statement/Q55787334-09B4BF7D-E906-4AED-B852-24F891C8B165
wd:statement/Q55787334-15381137-B2B3-4217-816D-60BE1889BD10
wd:statement/Q55787334-1CFB0B75-25D7-43BD-9A04-28EF95A19266
wd:statement/Q55787334-207C2805-2B52-43AB-A3D8-F8F861C15852
wd:statement/Q55787334-270D5E43-DAFA-4EC1-9EF1-1BC969A7B4D9
wd:statement/Q55787334-295FD281-74DA-41E5-A66F-1EE5958BADB3
wd:statement/Q55787334-2B270C93-262C-440C-8A95-9C915A898174
wd:statement/Q55787334-358FFE97-206C-437D-9564-3818CD73860A
wd:statement/Q55787334-391ED6DD-A29F-45E3-B2D8-278376CE8DA9
wd:statement/Q55787334-43E2770E-41A3-4839-972A-AC894BAA175F
wd:statement/Q55787334-4D5BFC16-EAE5-4397-A107-2295DD4B266B
wd:statement/Q55787334-67A67F60-487D-4464-BF72-A020AF3987A1
wd:statement/Q55787334-8DC71492-60F0-4660-858F-5E4300D5CB29
wd:statement/Q55787334-8E4353D4-CCE6-4BD9-AB9D-93B50048F446
wd:statement/Q55787334-9786C3FC-DBC9-41AA-B660-389A56FBABEC
wd:statement/Q55787334-9E8C4AAD-BC32-409D-89CF-A0B8B8B0DD4E
wd:statement/Q55787334-AE193840-B8B7-4EBB-B5FA-3E9C757FF429
wd:statement/Q55787334-B06F732A-4E2C-4962-AAA1-BAFB1FF0BF43
wd:statement/Q55787334-B37DD823-3D6A-405A-A498-B41D550B11CE
wd:statement/Q55787334-BF31578B-2E90-4DC5-8969-DAFB1A3F53BF
wd:statement/Q55787334-C7BAFF7D-D56C-4E48-A409-F3A0898914DE
wd:statement/Q55787334-E5909C80-5252-4D67-B118-DAB848D97381
wd:statement/Q55787334-E930581C-0598-47C6-9CE8-6587D1C7BA53
wd:statement/Q55787334-EA073DD0-53C6-46CA-B39B-01A6C89A6A44
wd:statement/Q55787334-F143E612-A60A-4E92-8B58-A8FEAE06B60A
wd:statement/Q55787334-F4DF7DE3-168B-4F5C-91DD-F8E3446A1A59
wd:statement/Q55787334-F75AEC3D-0FE4-49A3-9C6B-5B7D0DAC8D74
p:P279 wd:statement/Q55787334-3A8AD7FF-000F-4C8E-9ED9-CD9126080697
p:P2888 wd:statement/Q55787334-E71FE54E-5537-47CF-B6A6-1DF1B291ED49
p:P2892 wd:statement/Q55787334-D6668012-AEA6-45D6-9133-49119408BAA3
p:P31 wd:statement/Q55787334-65920F87-CA37-4C40-B3B1-377417B2A4D8
p:P5270 wd:statement/Q55787334-CFCFC248-CB83-428C-8186-650202372FC1
p:P7329 wd:statement/Q55787334-e2f73eee-322a-4e71-a224-21df773bc3b9
p:P7807 wd:statement/Q55787334-18350EBD-D7E2-4208-87AB-D2AAB1A87E3A
p:P910 wd:statement/Q55787334-63889f20-458c-4c80-9b28-1ba69f87c941
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0017758>
wdt:P14914 "D309827"
wdt:P1550 "309827"
wdt:P2293 DHFR
CBLIF
MTHFR
MTR
SLC19A2
SLC19A3
FOLR1
HCFC1
MTRR
PRDX1
ABCD4
SLC19A1
TCN2
CUBN
MTHFS
FTCD
MMACHC
TPK1
MMADHC
CD320
BCO1
LMBRD1
THAP11
SLC25A19
AMN
SLC46A1
MMAA
MMAB
wdt:P279 disorder of metabolite absorption and transport
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_309827>
wdt:P2892 "C5681037"
wdt:P31 type of disease
wdt:P5270 "MONDO_0017758"
wdt:P7329 "5C63"
wdt:P7807 "1112006621"
wdt:P910 wd:Q7867679
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data from SPARQL profile: Wikidata