@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU
> .
@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:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_head
{
this:
np:hasAssertion
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_assertion
;
np:hasProvenance
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_provenance
;
np:hasPublicationInfo
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_assertion
a
np:Assertion
.
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_provenance
a
np:Provenance
.
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGNf0bddd242f0fc5d0e34ab37e7c97221f
sio:SIO_000628
miriam-gene:7157
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_provenance
{
dgn-np:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_assertion
dcterms:description
"[Inactivation of the p53 pathway may, therefore, be important in children with ALL who fail to respond to treatment and may be useful for the early identification of children requiring alternative therapies.]. 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:8562942
;
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:NP246262.RA5Sk3GJYEI96mB5Cg2cFhiuC9C18iYEGrmaKtxnQ_ijU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}