@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs
> .
@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/v4.0.0/void/
> .
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_head
{
this:
np:hasAssertion
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_assertion
;
np:hasProvenance
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_provenance
;
np:hasPublicationInfo
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_assertion
a
np:Assertion
.
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_provenance
a
np:Provenance
.
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_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:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_provenance
{
dgn-np:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_assertion
dcterms: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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP957103.RAQz0Ml10MMISEIZ7Y4P_Mi5uwoKJk6NJKqtWxY6DvRLs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:58+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}