@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs
> .
@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:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_head
{
this:
np:hasAssertion
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_assertion
;
np:hasProvenance
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_provenance
;
np:hasPublicationInfo
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_assertion
a
np:Assertion
.
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_provenance
a
np:Provenance
.
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGNf6390de88a6ae9c10ff3b95d9cef4f5f
sio:SIO_000628
miriam-gene:4846
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_provenance
{
dgn-np:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_assertion
dcterms:description
"[To investigate the association of two common genetic polymorphisms of the gene encoding for endothelial nitric oxide synthase (Nos3), the enzyme catalyzing the production of nitric oxide (NO), with occurrence of the polycystic ovary syndrome (PCOS).]. 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:18804337
;
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:NP540313.RAydz86eBGa8yeNhslOKCdBaMq6Qn4mwshKiXI4fshqJs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:26+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" .
}