@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4
> .
@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/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4130_assertion
a
np:Assertion
.
dgn-np:NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4130_provenance
a
np:Provenance
.
dgn-np:NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:7056
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGN79c3d96b7553771a0a90bd8c37631379
sio:SIO_000628
miriam-gene:7056
,
lld:C0002895
;
a
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.
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dgn-np:NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4130_provenance
{
dgn-np:NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4130_assertion
dcterms:description
"[It is expected that this study will yield important information on genetic risk factors for the cerebrovascular disease phenotype in SCD by clarifying the role of candidate genes in the development of high TCD. The genomewide screen for a large number of ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:12871600
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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 .
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dgn-np:NP62550.RAilKky38x02l2nHInL4wOnweg-Xvzcx-jqf0CnTrWko4130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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"v3.0.0" .
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