@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_provenance
;
np:hasPublicationInfo
dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_assertion
a
np:Assertion
.
dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_provenance
a
np:Provenance
.
dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:4842
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN670b448bc45dbaecb7a264e90160527e
sio:SIO_000628
miriam-gene:4842
,
lld:C0011860
;
a
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.
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dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_provenance
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dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_assertion
dcterms:description
"[To analyze the functional significance of the G894T polymorphism of NOS3, the gene encoding endothelial nitric oxide synthase (NOS), we assessed basal nitric oxide activity and the amount of oxidative stress in the renal circulation of patients with type 2 diabetes.]. 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:18622262
;
prov:wasDerivedFrom
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;
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 .
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dgn-np:NP741033.RAVDZjFKr4powPtf_MYbGOmSeMPAOPY72T6WldgjINPeM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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
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pav:authoredBy
<
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> , <
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> , <
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
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"v2.1.0" .
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