@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE
> .
@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:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_head
{
this:
np:hasAssertion
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_assertion
;
np:hasProvenance
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_provenance
;
np:hasPublicationInfo
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_assertion
a
np:Assertion
.
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_provenance
a
np:Provenance
.
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_assertion
{
miriam-gene:28956
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNa8c62f8050c9d2457af6dbd55dae5de2
sio:SIO_000628
miriam-gene:28956
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_provenance
{
dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_assertion
dcterms:description
"[Since the incidence and clinical implications of abnormalities of TP53, CDKN2A (encoding for p16 and p14) and MDM2 genes (chromosome 12) in multiple myeloma (MM) is not clear, we investigated allelic loss at the former two loci and gain at the latter locus in a series of 82 MM patients.]. 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:12745272
;
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 .
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dgn-np:NP455912.RA4QZPhzDA9FHrfvcWFUgNnKaF_-nkBIcpK80CPZG3sBE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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
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
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"v2.1.0" .
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