@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU
> .
@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:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_head
{
this:
np:hasAssertion
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_assertion
;
np:hasProvenance
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_provenance
;
np:hasPublicationInfo
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_assertion
a
np:Assertion
.
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_provenance
a
np:Provenance
.
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_assertion
{
miriam-gene:29107
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGN69c78ba7857402ece0d6674da6a17e8c
sio:SIO_000628
miriam-gene:29107
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_provenance
{
dgn-np:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_assertion
dcterms:description
"[Here we report, for the first time in the literature, the high incidences of p16 and p15 alterations in MM, not by homozygous deletions or mutations, but solely by hypermethylation of the 5' CpG islands, which may be a specific mechanism in this disease.]. 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:9116295
;
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:NP353794.RA4zzJSIrhh5EkvS9cKcC_2IDh_QeLSY1Fre33PE49lVU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}