@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis
> .
@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:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_head
{
this:
np:hasAssertion
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_assertion
;
np:hasProvenance
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_provenance
;
np:hasPublicationInfo
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_assertion
a
np:Assertion
.
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_provenance
a
np:Provenance
.
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_assertion
{
miriam-gene:1666
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGNbc10180a1524022702f01839240bc1fa
sio:SIO_000628
miriam-gene:1666
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_provenance
{
dgn-np:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_assertion
dcterms:description
"[Epigenetic silencing of NADPH oxidases by hypermethylation of their promoter region or of the genes required for their assembly and activity occurs in diseases, such as lung cancer, and may represent an early stage of neoplastic transformation.]. 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:23126619
;
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:NP901838.RAQW1K8bd--ickU5ac_BZGj1VFVFS5tSasl9979kbCfis130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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" .
}