@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg
> .
@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:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_head
{
this:
np:hasAssertion
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion
;
np:hasProvenance
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance
;
np:hasPublicationInfo
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion
a
np:Assertion
.
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance
a
np:Provenance
.
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion
{
miriam-gene:4855
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGN2a5ab3a23c15461945c0e500f0077355
sio:SIO_000628
miriam-gene:4855
,
lld:C0011265
;
a
sio:SIO_001121
.
}
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_provenance
{
dgn-np:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_assertion
dcterms:description
"[Mutations in the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), which is clinically characterised by recurrent ischemic strokes, migraine with aura, psychiatric symptoms, cognitive decline and dementia.]. 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:16807713
;
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:NP556039.RAAo14NuoLTKNz2rxcGq_iY0iBKvKcO-UtWv74UVHAjvg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:35+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" .
}