@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw
> .
@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/v4.0.0/void/
> .
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_head
{
this:
np:hasAssertion
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_assertion
;
np:hasProvenance
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_provenance
;
np:hasPublicationInfo
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_assertion
a
np:Assertion
.
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_provenance
a
np:Provenance
.
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C1883486
a
ncit:C7057
.
dgn-gda:DGN6ac4747f786df80cca52e278b9343069
sio:SIO_000628
miriam-gene:1586
,
lld:C1883486
;
a
sio:SIO_001122
.
}
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_provenance
{
dgn-np:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP579837.RAQU5smGkEz-NTkWN1cqo5wnqO5QkD-66EK9fUvTGCNkw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:08+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}