@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_assertion
a
np:Assertion
.
dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_provenance
a
np:Provenance
.
dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_assertion
{
miriam-gene:1805
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNe673a4257162a51aef28c859921f3a72
sio:SIO_000628
miriam-gene:1805
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_provenance
{
dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_assertion
dcterms:description
"[In summary, our data reveal a systemic DNA methylation pathway defect in TRAMP reminiscent of human prostate cancer, supporting the use of this model to investigate the functional role of DNA methylation pathway alterations in prostate cancer development.]. 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:17178860
;
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 .
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dgn-np:NP344398.RA5pw5LQEYm9QAQ2QHEcEQwizOOAiAbXhu91eIXNiAzQY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
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pav:version
"v2.1.0" .
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