@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o
> .
@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:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_head
{
this:
np:hasAssertion
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_assertion
;
np:hasProvenance
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_provenance
;
np:hasPublicationInfo
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_assertion
a
np:Assertion
.
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_provenance
a
np:Provenance
.
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN39f0d370f5b93ff72b1441551fadbf20
sio:SIO_000628
miriam-gene:4846
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_provenance
{
dgn-np:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_assertion
dcterms:description
"[The T-786C polymorphism of the eNOS gene appears to be an independent risk factor for CAD in Chinese Hans. This finding requires confirmation in prospective studies and in studies of other populations.]. 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:20215811
;
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:NP167119.RAq91pVnXfvfgPd4tFH_Xsk4lTRnyYOCD8lRVzElyeJ3o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:03+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" .
}