@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_head
{
this:
np:hasAssertion
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_assertion
;
np:hasProvenance
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_assertion
a
np:Assertion
.
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_provenance
a
np:Provenance
.
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0007103
a
ncit:C7057
.
dgn-gda:DGN39858cace7e037b9ef25be6b5a96b90b
sio:SIO_000628
miriam-gene:1586
,
lld:C0007103
;
a
sio:SIO_001122
.
}
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_provenance
{
dgn-np:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_assertion
dcterms:description
"[The position -34T/C variant in CYP17A1 appears to be associated with reduced risk of endometrial cancer, with those homozygous for the variant allele having about half the risk of those homozygous for the wild type.]. 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:17110639
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP344494.RAThNnWrThG-pqA4j0hwSjymHUInQbIO_BkFa3DPS9-kQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:58+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}