@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo
> .
@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:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_head
{
this:
np:hasAssertion
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_assertion
;
np:hasProvenance
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_provenance
;
np:hasPublicationInfo
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_assertion
a
np:Assertion
.
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_provenance
a
np:Provenance
.
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN5b880308d784d851326fc617a29b5012
sio:SIO_000628
miriam-gene:4846
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_provenance
{
dgn-np:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_assertion
dcterms:description
"[Taken together, our results do not support the previous observation that the molecular variant of the eNOS gene may confer principal susceptibility for essential hypertension but rather suggest the existence of sampling variation.]. 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:10205226
;
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:NP377460.RAafxTVY__HpEKleWkX2a9q1jkO6twEFiPUv5RYfLsSBo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:41+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" .
}