@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0
> .
@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 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:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_head
{
this:
np:hasAssertion
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_assertion
;
np:hasProvenance
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_provenance
;
np:hasPublicationInfo
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_assertion
a
np:Assertion
.
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_provenance
a
np:Provenance
.
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGN563d59f0663cd525283f5b9c43159f85
sio:SIO_000628
miriam-gene:7248
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_provenance
{
dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_assertion
dc:description
"[Our results suggest that there is a heterogeneous, non-systematic but almost universal presence of activated oncogenes and tumour suppressor genes in the plasma cells of patients with multiple myeloma and that disease progression is associated with the accumulation of a variety of secondary genetic changes which confer increased malignant behaviour.]. 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:7696921
;
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:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:38+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}