@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E
> .
@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:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_head
{
this:
np:hasAssertion
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_assertion
;
np:hasProvenance
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_provenance
;
np:hasPublicationInfo
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_assertion
a
np:Assertion
.
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_provenance
a
np:Provenance
.
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_assertion
{
miriam-gene:3690
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN89d307c3df2b6502701b26d667a251de
sio:SIO_000628
miriam-gene:3690
,
lld:C0004153
;
a
sio:SIO_001122
.
}
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_provenance
{
dgn-np:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_assertion
dcterms:description
"[, the 807T allele of GP Ia and the PlA2 allele of GP IIIa, and specially its combination, may confer an additional risk for development of carotid atherosclerosis and arterial thrombosis in type 2 diabetes.]. 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:20076847
;
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:NP71568.RAikTAvxH7zDWXTNlwuSfn9N2-J1bMhHVGFQWQ2fBaZ1E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:34+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" .
}