@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM
> .
@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:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_head
{
this:
np:hasAssertion
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_assertion
;
np:hasProvenance
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_provenance
;
np:hasPublicationInfo
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_assertion
a
np:Assertion
.
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_provenance
a
np:Provenance
.
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGN3494e7eb359838c918e5ff6d3feaf570
sio:SIO_000628
miriam-gene:3342
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_provenance
{
dgn-np:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_assertion
dcterms:description
"[Comparative genomic hybridization (CGH) was used to identify recurrent regions of DNA sequence loss and gain in 21 multiple myeloma (MM) and plasma cell leukemia (PCL) primary tumor specimens and cell lines.]. 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:9172003
;
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:NP625153.RA-bsi54TuIqAwo-eMfGDC27OwLvrTMjrzRXixAqOpziM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}