@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP873675.RAuk0HUD5Q6qhXCTZPkzvdg4oH0UZGsMhwPSaZ7V4LVDk
> .
@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
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;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP873675.RAuk0HUD5Q6qhXCTZPkzvdg4oH0UZGsMhwPSaZ7V4LVDk130_provenance
a
np:Provenance
.
dgn-np:NP873675.RAuk0HUD5Q6qhXCTZPkzvdg4oH0UZGsMhwPSaZ7V4LVDk130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP873675.RAuk0HUD5Q6qhXCTZPkzvdg4oH0UZGsMhwPSaZ7V4LVDk130_assertion
{
miriam-gene:3957
a
ncit:C16612
.
lld:C0242231
a
ncit:C7057
.
dgn-gda:DGN8511bffb6a228cbeaa1825ba7b244656
sio:SIO_000628
miriam-gene:3957
,
lld:C0242231
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.
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dgn-np:NP873675.RAuk0HUD5Q6qhXCTZPkzvdg4oH0UZGsMhwPSaZ7V4LVDk130_provenance
{
dgn-np:NP873675.RAuk0HUD5Q6qhXCTZPkzvdg4oH0UZGsMhwPSaZ7V4LVDk130_assertion
dcterms:description
"[We investigated the correlation between polymorphisms of the LTA, LGALS2, and PSMA6 genes and the severity of pathological coronary stenosis index (CSI) and MI in 1503 consecutive autopsy cases of Japanese elderly patients.]. 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:22310064
;
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:NP873675.RAuk0HUD5Q6qhXCTZPkzvdg4oH0UZGsMhwPSaZ7V4LVDk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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
<
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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