@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c
> .
@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:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_head
{
this:
np:hasAssertion
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_assertion
;
np:hasProvenance
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_provenance
;
np:hasPublicationInfo
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_assertion
a
np:Assertion
.
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_provenance
a
np:Provenance
.
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_assertion
{
miriam-gene:7020
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNb06e016b82970083ae2d687b95638b70
sio:SIO_000628
miriam-gene:7020
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_provenance
{
dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_assertion
dcterms:description
"[We have identified aberrant CpG DNA methylation as an epigenetic mark associated with TFAP2A silencing in human melanoma that could have significant implications for the therapy of human melanoma using epigenetic modifying drugs.]. 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:25625848
;
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:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:17+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}