@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_head
{
this:
np:hasAssertion
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_assertion
;
np:hasProvenance
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_provenance
;
np:hasPublicationInfo
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_assertion
a
np:Assertion
.
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_provenance
a
np:Provenance
.
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_assertion
{
miriam-gene:4855
a
ncit:C16612
.
lld:C0234958
a
ncit:C7057
.
dgn-gda:DGN357e3de1cc4299cebbd2124dfe96b90d
sio:SIO_000628
miriam-gene:4855
,
lld:C0234958
;
a
sio:SIO_001121
.
}
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_provenance
{
dgn-np:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_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-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP884025.RAFoveXfDz_136dE7mKsKOb3OEKwLAA-CPiZCUovoqaZE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}