@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM
> .
@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:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_head
{
this:
np:hasAssertion
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_assertion
;
np:hasProvenance
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_provenance
;
np:hasPublicationInfo
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_assertion
a
np:Assertion
.
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_provenance
a
np:Provenance
.
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN94619731fdaf8bc584af9f0dbbf4a078
sio:SIO_000628
miriam-gene:7157
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_provenance
{
dgn-np:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_assertion
dcterms:description
"[Fourteen patients with various leukemias were examined and two with acute lymphoblastic leukemia and one with Waldenström's macroglobulinemia were identified to have mutations in the coding region of the p53 gene.]. 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:1705829
;
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:NP172010.RABPjzVxMLTPraC3o71JIOMAQkN48g3k49vKxdDlbLMMM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}