@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY
> .
@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:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_head
{
this:
np:hasAssertion
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_assertion
;
np:hasProvenance
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_provenance
;
np:hasPublicationInfo
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_assertion
a
np:Assertion
.
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_provenance
a
np:Provenance
.
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_assertion
{
miriam-gene:83886
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNa0d1debd7410298409a6c2bbe2cdca98
sio:SIO_000628
miriam-gene:83886
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_provenance
{
dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_assertion
dcterms:description
"[Mutations in the Cbl family RING finger domain or linker sequence constitute important pathogenic lesions associated with not only preleukemic CMML, JMML, and other MPN, but also progression to AML, suggesting that impairment of degradation of activated tyrosine kinases constitutes an important cancer mechanism.]. 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:19901108
;
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:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}