@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_head
{
this:
np:hasAssertion
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_assertion
;
np:hasProvenance
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_assertion
a
np:Assertion
.
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_provenance
a
np:Provenance
.
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGNe2aae22a7bb0248fb792d7ffdbb02fdf
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001121
.
}
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_provenance
{
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_assertion
dcterms:description
"[Nonsynonymous mutations in the human prion protein (HuPrP) gene contribute to the conversion of HuPrP(C) to HuPrP(Sc) and amyloid formation which in turn leads to prion diseases such as familial Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:23527686
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP1063383.RAhssb9lkNPIN6pxU0oWhxS2jtS3_u6ti2yVhNN7eOshg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:48+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}