@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_assertion
;
np:hasProvenance
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_provenance
;
np:hasPublicationInfo
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_assertion
a
np:Assertion
.
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_provenance
a
np:Provenance
.
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_assertion
{
miriam-gene:867
a
ncit:C16612
.
lld:C0280449
a
ncit:C7057
.
dgn-gda:DGNef94cabe8ebc467919d740e2c3cd905c
sio:SIO_000628
miriam-gene:867
,
lld:C0280449
;
a
sio:SIO_001121
.
}
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_provenance
{
dgn-np:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_assertion
dcterms:description
"[In particular the detection and quantification of a copy-neutral loss of heterozygosity region located in chromosome 11q guided the search for point mutations in the CBL gene, thus allowing the escription of the novel missense mutation K382E and the demonstration of its selection during progression to secondary AML.]. 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:20674974
;
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:NP306487.RAzi_F6ELVN_nNmWGKYxNI0VjkLJMgT8y_O26vaMOB4xY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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
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"v2.1.0" .
}