@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U
> .
@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:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_head
{
this:
np:hasAssertion
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_assertion
;
np:hasProvenance
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_provenance
;
np:hasPublicationInfo
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_assertion
a
np:Assertion
.
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_provenance
a
np:Provenance
.
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_assertion
{
miriam-gene:2155
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNfb82f6b60686d8cd748dd0b6f8ae14bc
sio:SIO_000628
miriam-gene:2155
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_provenance
{
dgn-np:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_assertion
dcterms:description
"[There is evidence that Factor VII polymorphisms are markers of susceptibility to coronary artery disease (CAD), but two studies have suggested that there is no association between the degree of vessel disease and these polymorphisms.]. 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:15837082
;
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:NP443471.RA2oTPqEI4EzPXcsRAkfv1gesfz9aUbX1i3ICRdLfAI4U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}