@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ
> .
@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:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_head
{
this:
np:hasAssertion
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_assertion
;
np:hasProvenance
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_assertion
a
np:Assertion
.
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_provenance
a
np:Provenance
.
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0349639
a
ncit:C7057
.
dgn-gda:DGN253a80f27fd113d37226b6b5dfdcc026
sio:SIO_000628
miriam-gene:7157
,
lld:C0349639
;
a
sio:SIO_001121
.
}
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_provenance
{
dgn-np:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_assertion
dcterms:description
"[These data indicate that abnormalities of the p53 gene are rare in JMML and not responsible for acute transformation, but could be involved in the pathogenesis of some cases of JMML.]. 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:10520001
;
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:NP458614.RAIxszFEnGcNYJxYWo4HCxyrVXi0JAcfn-wvq03Yge7QQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:33+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" .
}