@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g
> .
@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:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_head
{
this:
np:hasAssertion
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_assertion
;
np:hasProvenance
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_provenance
;
np:hasPublicationInfo
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_assertion
a
np:Assertion
.
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_provenance
a
np:Provenance
.
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_assertion
{
miriam-gene:57379
a
ncit:C16612
.
lld:C1512409
a
ncit:C7057
.
dgn-gda:DGNaea4b4c0cfedfb6f5c91f47114579145
sio:SIO_000628
miriam-gene:57379
,
lld:C1512409
;
a
sio:SIO_001121
.
}
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_provenance
{
dgn-np:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_assertion
dcterms:description
"[Our findings suggest that the aberrant expression of AID is observed in human hepatocytes with several pathological settings, including chronic liver disease and HCC, which might enhance the genetic susceptibility to mutagenesis leading to hepatocarcinogenesis.]. 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:17066440
;
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:NP187648.RAzJ7HFrh-Z84VQXJtlUX_VdT_U5UTQyt2GlxxrW1Vn-g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}