@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA
> .
@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:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_head
{
this:
np:hasAssertion
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_assertion
;
np:hasProvenance
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_provenance
;
np:hasPublicationInfo
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_assertion
a
np:Assertion
.
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_provenance
a
np:Provenance
.
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0700095
a
ncit:C7057
.
dgn-gda:DGN94ac01f408df43919b415430b2ae26dd
sio:SIO_000628
miriam-gene:7157
,
lld:C0700095
;
a
sio:SIO_001121
.
}
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_provenance
{
dgn-np:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_assertion
dcterms:description
"[Our findings suggest that mutations of the p53 gene in ES might represent late genetic events related to tumor progression, and that aberrations of the p53 gene might not be involved in the development or the progression of NB.]. 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:8221663
;
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:NP217326.RAygCBqbpl0QYjtRXesNb84Vw5k2o8vrY-827icRCRiSA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}