@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA
> .
@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:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_head
{
this:
np:hasAssertion
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_assertion
;
np:hasProvenance
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_provenance
;
np:hasPublicationInfo
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_assertion
a
np:Assertion
.
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_provenance
a
np:Provenance
.
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGN03070dbabf01c622b71aa5656d0e43dd
sio:SIO_000628
miriam-gene:4846
,
lld:C0018801
;
a
sio:SIO_001122
.
}
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_provenance
{
dgn-np:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_assertion
dcterms:description
"[Our data show in failing human myocardium that the T(-786)-->C promoter polymorphism is associated with reduced eNOS expression, whereas the G(894)-->T polymorphism of exon 7 is not associated with change in either eNOS mRNA or protein expression. Reduced eNOS expression associated with the promoter polymorphism may contribute to the vascular, contractile, and autonomic responses to ventricular failure.]. 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:20350698
;
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:NP68961.RADmFMkhwYM4hYgBmETnNcxaw7FY4qmSmz9OvrFqzCEdA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:33+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" .
}