@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg
> .
@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:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_head
{
this:
np:hasAssertion
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_assertion
;
np:hasProvenance
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_provenance
;
np:hasPublicationInfo
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_assertion
a
np:Assertion
.
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_provenance
a
np:Provenance
.
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_assertion
{
miriam-gene:83478
a
ncit:C16612
.
lld:C0278701
a
ncit:C7057
.
dgn-gda:DGN4cc454ed12f2c1b03ae6d833cdccf227
sio:SIO_000628
miriam-gene:83478
,
lld:C0278701
;
a
sio:SIO_001121
.
}
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_provenance
{
dgn-np:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_assertion
dcterms:description
"[Because of the similarities between the p53 and p73 genes and the high frequency of mutation of p53, this study was designed to investigate the p73 gene in patients with gastric adenocarcinoma.]. 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:12560466
;
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:NP539844.RAu1OgOQtY-ETzj8IwKAw9Sp6BHlTbcCL1zY8cp88oDmg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}