@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ
> .
@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 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:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_head
{
this:
np:hasAssertion
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion
;
np:hasProvenance
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion
a
np:Assertion
.
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_provenance
a
np:Provenance
.
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion
{
miriam-gene:2146
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNfc8a1d762c941a86dae09a7cf4f40f9b
sio:SIO_000628
miriam-gene:2146
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_provenance
{
dgn-np:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_assertion
dct:description
"[ We have possibly identified haplotypes which mark alleles that have a beneficial effect on the development of prostate cancer. Moreover, our results suggest that genetic variations of the EZH2 gene are not responsible for the linkage of 7q to aggressive prostate cancer.]. 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:16015586
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44640.RAuXFH6dX-AREe9lEzYkNLPrvkfv2cURXcvYet-uw1BfQ130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}