@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg
> .
@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:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_head
{
this:
np:hasAssertion
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_assertion
;
np:hasProvenance
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_provenance
;
np:hasPublicationInfo
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_assertion
a
np:Assertion
.
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_provenance
a
np:Provenance
.
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0026470
a
ncit:C7057
.
dgn-gda:DGNf8373a7a195cfd750cdcc28fbcea6bd2
sio:SIO_000628
miriam-gene:6520
,
lld:C0026470
;
a
sio:SIO_001121
.
}
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_provenance
{
dgn-np:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_assertion
dcterms:description
"[Chromosomal translocations involving the immunoglobulin heavy chain gene (IgH) and nonrandom protooncogene loci are the hallmark of genetic alterations found not only in multiple myeloma (MM), but also in premalignant stages of MM, including monoclonal gammopathy of undetermined significance (MGUS) and smoldering myeloma (SMM).]. 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:12824903
;
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:NP394494.RABp2d00mJVK2YH1Z2Hp4wNKQ5tbhdrPzuzhd-enKmoJg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}