@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU
> .
@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:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_head
{
this:
np:hasAssertion
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_assertion
;
np:hasProvenance
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_provenance
;
np:hasPublicationInfo
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_assertion
a
np:Assertion
.
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_provenance
a
np:Provenance
.
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_assertion
{
miriam-gene:29107
a
ncit:C16612
.
lld:C0862196
a
ncit:C7057
.
dgn-gda:DGNdec19f079792bf86f410aa9686e38e7e
sio:SIO_000628
miriam-gene:29107
,
lld:C0862196
;
a
sio:SIO_001121
.
}
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_provenance
{
dgn-np:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_assertion
dcterms:description
"[This study suggests that abnormalities of the P15 and P16 genes are common in both early and advanced stages of mycosis fungoides and Sezary syndrome and that these genes may be inactivated by allelic loss and aberrant promoter methylation.]. 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:11874489
;
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:NP220856.RAgjR4ZPcnVYvDx3IyoISoGVgAtxipWcvbmC1hDw__6CU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}