@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74
> .
@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:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_head
{
this:
np:hasAssertion
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_assertion
;
np:hasProvenance
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_provenance
;
np:hasPublicationInfo
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_assertion
a
np:Assertion
.
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_provenance
a
np:Provenance
.
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_assertion
{
miriam-gene:10544
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGNe8ec391e64992f91904fa7018758117d
sio:SIO_000628
miriam-gene:10544
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_provenance
{
dgn-np:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_assertion
dcterms:description
"[Our findings showed that the EPCR 23bp insertion is very rare in both patients with VTE and the general population and failed to support an association between the EPCR 23bp insertion and an increased risk of VTE.]. 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:11776299
;
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:NP393611.RA_DAlcz_rLmNEfbem3ZQxfVi2ncD7jaVquOQmwJd0v74130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}