@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_assertion
;
np:hasProvenance
dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_provenance
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np:hasPublicationInfo
dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_assertion
a
np:Assertion
.
dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_provenance
a
np:Provenance
.
dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:6696
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN1ada33460daf1e1c39c46e3a7e36bda9
sio:SIO_000628
miriam-gene:6696
,
lld:C0027051
;
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sio:SIO_001121
.
}
dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_provenance
{
dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_assertion
dcterms:description
"[We aimed at associating common osteopontin (OPN) gene variants with cardiovascular disease phenotypes.We scanned the OPN gene in 190 chromosomes from myocardial infarction (MI) patients and identified five variants in the promoter, three synonymous and one non-synonymous variant.]. 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:19281985
;
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 .
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dgn-np:NP457213.RA-1KgrC04CvSOPThyKBJzzb_KqGKkMmDyUYuKqOc9OmE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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
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dgn-void:disgenetrdf
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"v2.1.0" .
}