@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw
> .
@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 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:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_head
{
this:
np:hasAssertion
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_assertion
;
np:hasProvenance
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_provenance
;
np:hasPublicationInfo
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_assertion
a
np:Assertion
.
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_provenance
a
np:Provenance
.
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN1a610ea84ec48d1fbdcf1225b20cdde0
sio:SIO_000628
miriam-gene:4846
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_provenance
{
dgn-np:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_assertion
dc:description
"[Endothelial nitric oxide synthase (eNOS) gene polymorphisms have been associated with the pathogenesis of cardiovascular diseases, but few studies have evaluated the role of eNOS haplotypes on the risk and prognosis of heart failure (HF).]. 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:22290017
;
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:NP155967.RABNxvcEFnU1q0QkAhgyDVDh4q8Njop1Y8DnoG9IMb3Yw130_publicationInfo
{
this:
dc:created
"2014-10-02T12:33:24+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}