SHMARQL

transmissible spongiform encephalopathy

<http://www.wikidata.org/entity/Q703961>

group of brain diseases induced by prion proteins
rdfs:label
"transmissible spongiform encephalopathy"@en
skos:altLabel
"Prion disease"@en
"Prion disease pathway"@en
"Prion protein disease"@en
"Spongiform Encephalopathy"@en
"TSE"@en
"Transmissible spongiform encephalopathy"@en
"human prion disease"@en
"prion diseases"@en
"prion induced disorder"@en
schema:description
"group of brain diseases induced by prion proteins"@en
schema:dateModified "2026-10-24T00:26:51+00:00"^^xsd:dateTime
schema:version 2560165896
wikibase:identifiers 36
39
wikibase:sitelinks 34
wikibase:statements 59
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p:P8313 wd:statement/Q703961-A1D49D1E-2E00-44F7-AFB0-4574E28FAF3C
p:P8408 wd:statement/Q703961-791EE090-2191-43EA-8D58-0341B5A49B98
p:P910 wd:statement/Q703961-03BF61B8-480E-48A8-B1E3-039E67B81EC4
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D017096>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0018926>
p:direct-normalized/P6366 <https://makg.org/entity/2776797465>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00061>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C01.207.800>
<http://id.nlm.nih.gov/mesh/C10.228.228.800>
<http://id.nlm.nih.gov/mesh/C10.574.843>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:649>
p:direct-normalized/P8408 <http://kbpedia.org/kko/rc/Transmissible-spongiform-encephalopathy>
wdt:P10283 "C2776797465"
wdt:P11143 "Transmissible spongiform encephalopathy"
wdt:P1193 0.000005^^xsd:decimal
wdt:P11956 "0004720"
wdt:P1325 <http://www.nanbyou.or.jp/entry/5370>
wdt:P1417 "science/spongiform-encephalopathy"
wdt:P1424 Template:Prion diseases
wdt:P14914 "D56970"
wdt:P1550 "56970"
wdt:P1692 "046.19"
wdt:P1748 "C128346"
"C27585"
wdt:P1995 infectious diseases
wdt:P2293 PRNP
SEMA3A
wdt:P279 neurodegenerative disease with dementia
encephalopathy
wdt:P2841 adult onset
wdt:P2888 <http://identifiers.org/doid/DOID:649>
<http://purl.obolibrary.org/obo/DOID_649>
<http://www.orpha.net/ORDO/Orphanet_56970>
wdt:P2892 "C0162534"
"C0751645"
wdt:P31 type of disease
designated intractable/rare disease
rare disease
wdt:P3219 "encephalopathies-spongiformes"
wdt:P3365 "est_res-02eba6b2-a833-11de-baff-0016357eee51"
wdt:P373 "Transmissible spongiform encephalopathies"
wdt:P3827 "prion-diseases"
wdt:P4229 "A81.0"
"A81.1"
"A81.8"
"A81.9"
wdt:P4233 "Transmissible-spongiform-encephalopathy"
wdt:P4746 "057535"
wdt:P486 "D017096"
wdt:P493 "046"
wdt:P494 "A81"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0018926"
wdt:P557 "25165"
wdt:P6058 "medical/encéphalopathie_spongiforme_subaiguë_transmissible/12768"
wdt:P6366 "2776797465"
wdt:P646 "/m/01j5jz"
wdt:P665 "H00061"
wdt:P672 "C01.207.800"
"C10.228.228.800"
"C10.574.843"
wdt:P673 "1168941"
wdt:P691 "ph137022"
"ph137024"
wdt:P699 "DOID:649"
wdt:P7329 "8E02"
wdt:P7807 "1965146397"
wdt:P828 prion
wdt:P8313 "TSE"
wdt:P8408 "Transmissible-spongiform-encephalopathy"
wdt:P910 Category:Transmissible spongiform encephalopathies
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