@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_head
{
this:
np:hasAssertion
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_assertion
;
np:hasProvenance
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_provenance
;
np:hasPublicationInfo
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_assertion
a
np:Assertion
.
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_provenance
a
np:Provenance
.
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_assertion
{
miriam-gene:4843
a
ncit:C16612
.
lld:C0151744
a
ncit:C7057
.
dgn-gda:DGN5419005ac3242e514a6c6592309e5fcc
sio:SIO_000628
miriam-gene:4843
,
lld:C0151744
;
a
sio:SIO_001122
.
}
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_provenance
{
dgn-np:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_assertion
dcterms:description
"[An association between polymorphism of iNOS gene (CCTTT)n, eNOS gene (Glu298Asp) with development of CHD and severity of CHF was shown. The polymorphism of eNOS gene (Glu298Asp) was associated with endothelial dysfunction.]. 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:20459417
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP97000.RA8OeuhxpoVyhtj5XfD38FjB2y19Bcy5bkTZoPEM70wME130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:33+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}