@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo
> .
@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:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_head
{
this:
np:hasAssertion
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_assertion
;
np:hasProvenance
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_provenance
;
np:hasPublicationInfo
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_assertion
a
np:Assertion
.
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_provenance
a
np:Provenance
.
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN04f68e846339dc5de9d867e53e1453d9
sio:SIO_000628
miriam-gene:1586
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_provenance
{
dgn-np:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_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-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:NP608846.RAkX3lJynUjhJPRwJ35d7NiJZbvY5BwztZbL4yKdhSrHo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}