@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_head
{
this:
np:hasAssertion
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_assertion
;
np:hasProvenance
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_assertion
a
np:Assertion
.
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_provenance
a
np:Provenance
.
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_assertion
{
miriam-gene:213
a
ncit:C16612
.
lld:C0391861
a
ncit:C7057
.
dgn-gda:DGNfdf6e84490426d366212a26ba76ec25d
sio:SIO_000628
miriam-gene:213
,
lld:C0391861
;
a
sio:SIO_001121
.
}
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_provenance
{
dgn-np:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_assertion
dcterms:description
"[The objective of this study was to investigate the mutational change in chromosome 13 (13q14) among Sudanese MM patients and to identify the association between extent of plasma cell infiltration in the bone marrow, albumin level and deletion of 13q14 by an analytical case control study.]. 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:26277665
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1292596.RADn0cnaza3lAE2uMu0YtrSwasUnxQRNbxfrt-9WANLpw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:32+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
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;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}