@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM
> .
@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:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_head
{
this:
np:hasAssertion
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_assertion
;
np:hasProvenance
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_provenance
;
np:hasPublicationInfo
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_assertion
a
np:Assertion
.
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_provenance
a
np:Provenance
.
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_assertion
{
miriam-gene:4056
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN0763d04e87df2c582bc4cc507de74667
sio:SIO_000628
miriam-gene:4056
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_provenance
{
dgn-np:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_assertion
dcterms:description
"[Using prospective, cross-sectional and case-control designs, we tested the hypothesis that hitherto unknown genetic variation, likely to affect the function of leukotriene C(4) synthase, is associated with risk of venous thromboembolism, ischemic stroke and myocardial infarction.]. 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:20456754
;
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:NP388738.RANJ7OuTIQJX0ZZ84A3V8Fm6XnG6CXML02Jl-ywKFWXMM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:51+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" .
}