@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w
> .
@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:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_head
{
this:
np:hasAssertion
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_assertion
;
np:hasProvenance
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_provenance
;
np:hasPublicationInfo
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_assertion
a
np:Assertion
.
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_provenance
a
np:Provenance
.
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_assertion
{
miriam-gene:57045
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGNf662c043473d8a88f4de390627d7bef8
sio:SIO_000628
miriam-gene:57045
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_provenance
{
dgn-np:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_assertion
dcterms:description
"[Molecular genetic analyses of human prostate cancer (CaP) has revealed frequent loss of specific chromosome regions suggesting the presence of putative tumor suppressor gene(s) (TSG) on these chromosome loci whose inactivation may play a role in prostate tumorigenesis.]. 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:10371356
;
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:NP889399.RA9kyBg3HIjRYFhmhFW7rv3EGOwcgYAbrsAFyvw5tDr3w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:06+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" .
}