@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw
> .
@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:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_head
{
this:
np:hasAssertion
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion
;
np:hasProvenance
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_provenance
;
np:hasPublicationInfo
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion
a
np:Assertion
.
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_provenance
a
np:Provenance
.
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion
{
miriam-gene:4552
a
ncit:C16612
.
lld:C1861172
a
ncit:C7057
.
dgn-gda:DGN7384c1b6f95a820923a1b20253048a17
sio:SIO_000628
miriam-gene:4552
,
lld:C1861172
;
a
sio:SIO_001122
.
}
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_provenance
{
dgn-np:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_assertion
dcterms:description
"[ Prothrombin and factor V polymorphisms increased the risk for VTE in women, independent from other established risk factors. Although hyperhomocysteinaemia also heightens this risk, common polymorphisms in two genes that are responsible for homocysteine remethylation do not. These findings are consistent with previous studies that included both men and women.]. 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:11806787
;
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:NP54233.RAhUyWRhn7Tc6yMQPo52-8eugn8jxY1W1f7LGXIOkaOBw130_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" .
}