@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg
> .
@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:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_head
{
this:
np:hasAssertion
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_assertion
;
np:hasProvenance
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_provenance
;
np:hasPublicationInfo
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_assertion
a
np:Assertion
.
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_provenance
a
np:Provenance
.
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_assertion
{
miriam-gene:4855
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNdc6c06b37d8e51d7ddde0af81a62c46c
sio:SIO_000628
miriam-gene:4855
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_provenance
{
dgn-np:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_assertion
dcterms:description
"[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene and is clinically characterized by recurrent stroke, cognitive decline, psychiatric disturbances and migraine.]. 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:21038489
;
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:NP200867.RAutIbhxeIezes5UFA9_5GnqYgz6bEUWBElffCvHPWJpg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}