@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo
> .
@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:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_head
{
this:
np:hasAssertion
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_assertion
;
np:hasProvenance
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_provenance
;
np:hasPublicationInfo
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_assertion
a
np:Assertion
.
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_provenance
a
np:Provenance
.
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN3706b8e1828af61a1ab53412f2ca4a3c
sio:SIO_000628
miriam-gene:7248
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_provenance
{
dgn-np:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_assertion
dcterms:description
"[Deletions of one copy of the RB and TP53 genes are less frequent as are mutations of the TP53 gene, and accumulating evidence suggests the presence of an additional tumour suppressor gene on chromosome 17p, which is frequently inactivated in 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:7621457
;
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:NP220088.RAGJQJAFttdX7qbIOzwXBpzwRKE5GwzzQfaVdPuuZWlRo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}