@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw
> .
@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:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_head
{
this:
np:hasAssertion
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_assertion
;
np:hasProvenance
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_provenance
;
np:hasPublicationInfo
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_assertion
a
np:Assertion
.
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_provenance
a
np:Provenance
.
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0026499
a
ncit:C7057
.
dgn-gda:DGN949c435a897b322f8055bd2e49314bc8
sio:SIO_000628
miriam-gene:7157
,
lld:C0026499
;
a
sio:SIO_001121
.
}
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_provenance
{
dgn-np:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_assertion
dcterms:description
"[The fact that P53 gene mutations occurred more often in patients with 17p monosomy seems to support the recessive model of tumor suppressive activity of the P53 gene rather than the dominant model, in which alteration of only one allele is sufficient for the development of malignancy.]. 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:1912553
;
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:NP712588.RApbdc-W-nCIOFRwd59uI7J0U0YdjmPU12cw2whT-cnHw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:08+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" .
}