@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs
> .
@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:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_head
{
this:
np:hasAssertion
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_assertion
;
np:hasProvenance
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_provenance
;
np:hasPublicationInfo
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_assertion
a
np:Assertion
.
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_provenance
a
np:Provenance
.
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_assertion
{
miriam-gene:23038
a
ncit:C16612
.
lld:C0085096
a
ncit:C7057
.
dgn-gda:DGN50275933c9ad663fc28ae0177bacf26a
sio:SIO_000628
miriam-gene:23038
,
lld:C0085096
;
a
sio:SIO_001121
.
}
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_provenance
{
dgn-np:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_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:NP713791.RATjHuExqMcXk4IcONuka3E3XKgglC6QRhn8u4kPw-LVs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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" .
}