@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY
> .
@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:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_head
{
this:
np:hasAssertion
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_assertion
;
np:hasProvenance
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_provenance
;
np:hasPublicationInfo
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_assertion
a
np:Assertion
.
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_provenance
a
np:Provenance
.
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGNc4b8d4b2d360fd1a26da6c2441cf7427
sio:SIO_000628
miriam-gene:7157
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_provenance
{
dgn-np:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_assertion
dcterms:description
"[p53 mutations predominated in lymphoid leukaemia and were several fold more frequent in leukaemia in relapse than in the de novo disease, were associated with loss of the normal p53 allele (monosomy 17) in > 50% of cases and carried a poor prognosis in AML, MDS and chronic lymphatic leukaemia and a 3.8-fold increase risk of death in T cell acute lymphocytic leukaemia.]. 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:9279367
;
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:NP160379.RA1eS-8DAokAnDUGeNK4HgWiLHIt4FgWqjv1fkqsnMGHY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}