@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M
> .
@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:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_head
{
this:
np:hasAssertion
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_assertion
;
np:hasProvenance
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_provenance
;
np:hasPublicationInfo
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_assertion
a
np:Assertion
.
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_provenance
a
np:Provenance
.
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_assertion
{
miriam-gene:4878
a
ncit:C16612
.
lld:C0007820
a
ncit:C7057
.
dgn-gda:DGN521dc188f5641b0bb157b3657bdb658c
sio:SIO_000628
miriam-gene:4878
,
lld:C0007820
;
a
sio:SIO_001122
.
}
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_provenance
{
dgn-np:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_assertion
dcterms:description
"[The frequency of this variant was similar in both groups and across the different stroke subtypes. The ANP gene G664A polymorphism is therefore unlikely to be an important risk factor for ischemic stroke in this population.]. 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:11706124
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP53756.RAOgidjwAGaHhTchHy_B9omZ16bK9P4EnFTY4Ztjn2W0M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}