@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw
> .
@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:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_head
{
this:
np:hasAssertion
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_assertion
;
np:hasProvenance
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_provenance
;
np:hasPublicationInfo
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_assertion
a
np:Assertion
.
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_provenance
a
np:Provenance
.
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_assertion
{
miriam-gene:842
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN25f509c4decfcfb3f1e190b6fe166e8e
sio:SIO_000628
miriam-gene:842
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_provenance
{
dgn-np:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_assertion
dcterms:description
"[Our results support the hypothesis that variants of CASP9 may influence the susceptibility to prostate cancer and its progression to bone metastasis. CASP8 polymorphism may influence the progression of prostate cancer disease to a hormone refractory state.]. 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:20804486
;
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:NP90980.RAyj5RvmrsvPi-mxmW49jsocvv3PdZ8osjekKnCQ8D8Zw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}