@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M
> .
@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:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_head
{
this:
np:hasAssertion
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_assertion
;
np:hasProvenance
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_provenance
;
np:hasPublicationInfo
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_assertion
a
np:Assertion
.
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_provenance
a
np:Provenance
.
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_assertion
{
miriam-gene:4928
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN9cbd513e33431729e84fa0a2ad55068c
sio:SIO_000628
miriam-gene:4928
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_provenance
{
dgn-np:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_assertion
dcterms:description
"[Moreover, we found a high incidence of loss of heterozygosity at chromosome 21q22.3, where the ADAR2 locus is located, in NSCLC cell lines and primary tissues, suggesting that the downregulation of ADAR2 in lung cancer is associated with specific genetic losses.]. 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:22876301
;
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:NP387030.RAvTvlLw-gtduC_mP3dAS5D703SyTpytlcThVmrUND_1M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:50+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" .
}