@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs
> .
@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:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_head
{
this:
np:hasAssertion
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_assertion
;
np:hasProvenance
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_provenance
;
np:hasPublicationInfo
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_assertion
a
np:Assertion
.
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_provenance
a
np:Provenance
.
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_assertion
{
miriam-gene:4879
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNc6f4980e0894e84ec04ba263a0e25226
sio:SIO_000628
miriam-gene:4879
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_provenance
{
dgn-np:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_assertion
dcterms:description
"[The BNP expression was examined in hypoxic myocardium of patients undergoing coronary bypass grafting surgery, in patients with coronary artery disease and normal left ventricular function undergoing percutaneous transluminal intervention therapy, and in heart failure patients without coronary artery 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:12709407
;
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:NP245105.RAhHKP09ZwUOjhOiSvxgj0YRcEARcc6-0eDLJGRN1zVIs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}