@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA
> .
@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:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_head
{
this:
np:hasAssertion
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_assertion
;
np:hasProvenance
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_provenance
;
np:hasPublicationInfo
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_assertion
a
np:Assertion
.
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_provenance
a
np:Provenance
.
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_assertion
{
miriam-gene:189
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGN282314d92c3f0273f4da2db67bbf6cf8
sio:SIO_000628
miriam-gene:189
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_provenance
{
dgn-np:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_assertion
dcterms:description
"[To explore the relationship between variation in AGT M235T gene and the development of the polycystic ovary syndrome (PCOS) and its sequelae, in the present study we evaluated AGT polymorphism M235T in women with PCOS and in a control group.]. 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:16275260
;
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:NP430686.RA-Vc8iQaYNk06V7CMrN9xqQWA4kk9_7plXRDNYu8jDGA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}