@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA
> .
@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:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_head
{
this:
np:hasAssertion
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_assertion
;
np:hasProvenance
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_provenance
;
np:hasPublicationInfo
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_assertion
a
np:Assertion
.
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_provenance
a
np:Provenance
.
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_assertion
{
miriam-gene:611
a
ncit:C16612
.
lld:C1512409
a
ncit:C7057
.
dgn-gda:DGN25b93d0a7078d319ae03caa536a5e816
sio:SIO_000628
miriam-gene:611
,
lld:C1512409
;
a
sio:SIO_001121
.
}
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_provenance
{
dgn-np:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_assertion
dcterms:description
"[It is possible that the mutations (BCP and preC mutations) associated with the HBeAg defective production might contribute to the diversity of mutations related to HBV persistence, playing an important role in hepatocarcinogenesis in this patient.]. 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:18051288
;
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:NP539069.RAFk9j-gNmIQvFS1TNuyAQOidnTJPA-voy8X6CJ0V0YQA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}