@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8
> .
@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:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_head
{
this:
np:hasAssertion
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_assertion
;
np:hasProvenance
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_provenance
;
np:hasPublicationInfo
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_assertion
a
np:Assertion
.
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_provenance
a
np:Provenance
.
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_assertion
{
miriam-gene:3973
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN75e43014290d9844be390124879a23af
sio:SIO_000628
miriam-gene:3973
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_provenance
{
dgn-np:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_assertion
dcterms:description
"[The aim of this study was to explore the polycystic ovary syndrome (PCOS) related single nucleotide polymorphisms (SNPs) rs13405728 (in gene LHCGR), rs13429458 (in gene THADA) and rs2479106 (in gene DENND1A) in women with endometrial carcinoma.]. 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:22902918
;
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:NP811241.RAtnQf50nkujlHUKb1qfwOG3E-z5E7mk4grUJvt8WI4n8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}