@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc
> .
@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:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_head
{
this:
np:hasAssertion
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_assertion
;
np:hasProvenance
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_provenance
;
np:hasPublicationInfo
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_assertion
a
np:Assertion
.
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_provenance
a
np:Provenance
.
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_assertion
{
miriam-gene:5054
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN1253ffd19615bd8efe2be70f8dfcdbf2
sio:SIO_000628
miriam-gene:5054
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_provenance
{
dgn-np:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_assertion
dcterms:description
"[The present data indicate that the A(-844)G gene polymorphism is not an independent risk factor of CAD and MI. The impact of this gene variation might be restricted to the extent of coronary artery disease for certain individuals who are at high risk for this disease.]. 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:12362251
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP51829.RA62CtdnBDIikuoq_a4Jj6tddEqKG5Tn7XgljvKu6Oorc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}