@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A
> .
@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:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_head
{
this:
np:hasAssertion
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_assertion
;
np:hasProvenance
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_assertion
a
np:Assertion
.
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_provenance
a
np:Provenance
.
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_assertion
{
miriam-gene:6319
a
ncit:C16612
.
lld:C0155626
a
ncit:C7057
.
dgn-gda:DGNf07cf03ce8e63bf498119b243fcce86e
sio:SIO_000628
miriam-gene:6319
,
lld:C0155626
;
a
sio:SIO_001121
.
}
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_provenance
{
dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_assertion
dcterms:description
"[In logistic regression analysis with age, body mass index, hypertension, diabetes, smoking and alcohol consumption as covariates, men with the TT genotype had an increased risk for SCD and AMI compared to CC carriers (OR=3.0, P=0.011; and OR=3.7, P=0.003).]. 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:16793047
;
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:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:36+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" .
}