@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg
> .
@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:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_head
{
this:
np:hasAssertion
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_assertion
;
np:hasProvenance
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_provenance
;
np:hasPublicationInfo
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_assertion
a
np:Assertion
.
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_provenance
a
np:Provenance
.
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGNb8ae1ba4d87dbf466e6b9e79664585e3
sio:SIO_000628
miriam-gene:1586
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_provenance
{
dgn-np:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_assertion
dcterms:description
"[When samples from 46 patients with endometriosis and 39 healthy controls were analysed, A2A2 type mutation of the CYP17 gene was observed to be more frequent in patients with endometriosis (34.8 versus 7.7%, P = 0.003).]. 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:20113968
;
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:NP321477.RApGf89SKHrOMAjZE_-Jz_mmBFYDQw4dd2D3QkY5Z2rCg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}