@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68
> .
@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:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_head
{
this:
np:hasAssertion
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_assertion
;
np:hasProvenance
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_provenance
;
np:hasPublicationInfo
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_assertion
a
np:Assertion
.
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_provenance
a
np:Provenance
.
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNed5c807ab3bf0f140af0222bdcbe6a0b
sio:SIO_000628
miriam-gene:7248
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_provenance
{
dgn-np:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_assertion
dcterms:description
"[The molecular basis of prostate cancer includes inheritable and somatic genetic changes (tumour suppressor genes, loss of heterozygosity, gene targets and regions of chromosomal gain, CpG island promoter methylation, invasion and metastasis suppressor genes, telomere shortening, and genetic instability).]. 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:12648986
;
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:NP315892.RAtA0VyrnpDZcTdbDyOxHJuA8uwc5RzkaJkvbNLBSIK68130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}