@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10
> .
@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:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_head
{
this:
np:hasAssertion
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_assertion
;
np:hasProvenance
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_provenance
;
np:hasPublicationInfo
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_assertion
a
np:Assertion
.
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_provenance
a
np:Provenance
.
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGN97f72f2ed2c610f10de62a1616a66824
sio:SIO_000628
miriam-gene:4854
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_provenance
{
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_assertion
dcterms:description
"[Mutations in the human Notch 3 gene cause the vascular stroke and dementia syndrome CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) characterized by degeneration of vascular smooth muscle cells and multiple small infarcts in the white and deep gray matter of the brain.]. 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:12126955
;
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:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}