@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0
> .
@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:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_head
{
this:
np:hasAssertion
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_assertion
;
np:hasProvenance
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_provenance
;
np:hasPublicationInfo
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_assertion
a
np:Assertion
.
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_provenance
a
np:Provenance
.
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN818d426d82cd0b83c40bf88e2cbec4f8
sio:SIO_000628
miriam-gene:2147
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_provenance
{
dgn-np:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_assertion
dcterms:description
"[We determined the prevalence of the G20210A mutation and prothrombin activity in 660 individuals, of whom 436 had angiographically documented severe coronary artery disease (CAD patients) and 224 had normal coronary angiography (CAD-free control subjects).]. 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:11369682
;
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:NP694596.RAfme7UQPl1nX9s83Cg_P-kZq4lFdzqUDcz2GOdRVqde0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:02+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" .
}