@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk
> .
@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:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_head
{
this:
np:hasAssertion
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_assertion
;
np:hasProvenance
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_provenance
;
np:hasPublicationInfo
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_assertion
a
np:Assertion
.
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_provenance
a
np:Provenance
.
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_assertion
{
miriam-gene:1401
a
ncit:C16612
.
lld:C0149871
a
ncit:C7057
.
dgn-gda:DGN20f448060d7415690a8a6b7d4ce02e6a
sio:SIO_000628
miriam-gene:1401
,
lld:C0149871
;
a
sio:SIO_001121
.
}
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_provenance
{
dgn-np:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_assertion
dcterms:description
"[CRP was also not independently associated with VTE in subgroups of patients (those with DVT without symptomatic PE, those with PE and patients without established risk factor) in multiple regression analysis.]. 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:15735799
;
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:NP775833.RAbx2w0Q6sdZnmHFwo-mPSUBW2EeoVmF5M59evyHM1TAk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}