@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M
> .
@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:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_head
{
this:
np:hasAssertion
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_assertion
;
np:hasProvenance
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_provenance
;
np:hasPublicationInfo
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_assertion
a
np:Assertion
.
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_provenance
a
np:Provenance
.
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_assertion
{
miriam-gene:5054
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN3de5e5d803a3e65cdbb15c4e27b18a18
sio:SIO_000628
miriam-gene:5054
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_provenance
{
dgn-np:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_assertion
dcterms:description
"[In a sample of both 83 healthy individuals and 105 young patients with coronary artery disease from Sweden, the frequency of the 4G allele is roughly 0.5, and those individuals homozygous for the 4G allele have higher levels of PAI-1 than those with other genotypes (29% higher).]. 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:1456879
;
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:NP182072.RAr9t7Gq23lJrRqwSqqbuw-EorbWq9iMAuR4UanlsAR0M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}