@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY
> .
@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:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_head
{
this:
np:hasAssertion
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion
;
np:hasProvenance
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance
;
np:hasPublicationInfo
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion
a
np:Assertion
.
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance
a
np:Provenance
.
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion
{
miriam-gene:2149
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN5ee272929b1eff61191496c1ea91a390
sio:SIO_000628
miriam-gene:2149
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_provenance
{
dgn-np:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_assertion
dcterms:description
"[The rs3024409 variant allele of F13A1 was associated with 1.66-fold increased risk of VTE, while the minor alleles of HABP2 rs6585234 and rs3862019, F2R rs253061 and rs153311, and PLAUR rs344782 were each associated with lower risk of VTE (hazard ratios in the range of 0.49-0.66).]. 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:19552680
;
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:NP853318.RAcNoIAxWGHNpPKTYySC-wAVA14AOKODZk1vULlmXx4DY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:42+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" .
}