@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_head
{
this:
np:hasAssertion
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_assertion
;
np:hasProvenance
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_assertion
a
np:Assertion
.
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_provenance
a
np:Provenance
.
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGNf92c8f2e5466870c740f127c8611e5dd
sio:SIO_000628
miriam-gene:7157
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_provenance
{
dgn-np:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_assertion
dcterms:description
"[Mutation and deletion of the p53 tumor suppressor gene are arguably the most prevalent among the multiple genetic alterations found in human bladder cancer, but these p53 defects are primarily associated with the advanced diseases, and their roles in bladder tumor initiation and in synergizing with oncogenes in tumor progression have yet to be defined.]. 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:14737103
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP429089.RAOBFPFhKLYcPK3bExhseDKZAC66FwP1WS7YPudhF_pGE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:59+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}