@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU
> .
@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:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_head
{
this:
np:hasAssertion
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_assertion
;
np:hasProvenance
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_provenance
;
np:hasPublicationInfo
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_assertion
a
np:Assertion
.
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_provenance
a
np:Provenance
.
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0740421
a
ncit:C7057
.
dgn-gda:DGN785a2dab26877a33de564551c7f6f715
sio:SIO_000628
miriam-gene:1594
,
lld:C0740421
;
a
sio:SIO_001121
.
}
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_provenance
{
dgn-np:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_assertion
dcterms:description
"[These results reveal the potential effect of the VDR gene on ovaries and uterus, and suggest that its SNPs can be used as predictors of genetic susceptibility for early surgical menopause and respective causal health problems.]. 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:17135034
;
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:NP790610.RA4skeSvU1xR30ONXFFfcFe1Gg_OWFZ9Se1LJ0adqfgqU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}