@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78
> .
@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:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_head
{
this:
np:hasAssertion
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_assertion
;
np:hasProvenance
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_provenance
;
np:hasPublicationInfo
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_assertion
a
np:Assertion
.
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_provenance
a
np:Provenance
.
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_assertion
{
miriam-gene:199720
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN2e735b68a1169990d8d85fb0eff74165
sio:SIO_000628
miriam-gene:199720
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_provenance
{
dgn-np:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_assertion
dcterms:description
"[The results support the hypothesis that the shorter alleles of CAG and GGN repeats in the AR gene are associated to an increased AR signalling intensity in human prostate cancer, and with more aggressive forms of the disease.]. 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:19095061
;
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:NP538238.RACHKG-dzEket5DKZaXLl4dY4wdJS8capWDCQITqmRC78130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}