@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI
> .
@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:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_head
{
this:
np:hasAssertion
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_assertion
;
np:hasProvenance
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_provenance
;
np:hasPublicationInfo
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_assertion
a
np:Assertion
.
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_provenance
a
np:Provenance
.
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_assertion
{
miriam-gene:23038
a
ncit:C16612
.
lld:C1704436
a
ncit:C7057
.
dgn-gda:DGN33684efcb95d1bc04ab58297609d4538
sio:SIO_000628
miriam-gene:23038
,
lld:C1704436
;
a
sio:SIO_001121
.
}
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_provenance
{
dgn-np:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_assertion
dcterms:description
"[The H2 haplotype of the P2Y12 receptor gene (P2RY12) has been found to be associated with maximal aggregation response to adenosine diphosphate (ADP) and with increased risk for peripheral arterial disease.]. 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:17803810
;
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:NP877173.RA6j19GoiguIEiWO58nPX2wueuxkfEBIh3GDwsLDIMARI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}