@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo
> .
@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:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_head
{
this:
np:hasAssertion
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_assertion
;
np:hasProvenance
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_assertion
a
np:Assertion
.
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_provenance
a
np:Provenance
.
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN9a6847a9db3dda46ceb42b7efa0c9f5d
sio:SIO_000628
miriam-gene:4854
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_provenance
{
dgn-np:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_assertion
dcterms:description
"[Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is the best understood cause of dominantly inherited stroke and results from NOTCH3 mutations that lead to NOTCH3 protein accumulation and selective arterial smooth muscle degeneration.]. 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:23028706
;
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:NP1017198.RAYzUCqldNdvHyR43omFg_4g4SF2P6Z4Qu4JJti6SJooo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:27+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" .
}