@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE
> .
@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:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_head
{
this:
np:hasAssertion
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_assertion
;
np:hasProvenance
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_assertion
a
np:Assertion
.
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_provenance
a
np:Provenance
.
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_assertion
{
miriam-gene:611
a
ncit:C16612
.
lld:C0023895
a
ncit:C7057
.
dgn-gda:DGN71669ab525048d7fc5a4fb472b714c86
sio:SIO_000628
miriam-gene:611
,
lld:C0023895
;
a
sio:SIO_001121
.
}
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_provenance
{
dgn-np:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_assertion
dcterms:description
"[In conclusion, our study suggests that the predominant HBV subgenotype HBV/D5 with high viral load and BCP mutations (double and triple) and high mutations in MHR region was significantly associated with advanced liver disease (LC and HCC) and might act as predictor of severe hepatic complications.]. 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:22820088
;
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:NP523383.RAX4wiRaIrKYgMhgMbPwEz--BaS379Mj4VJrXo9wWPVgE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:11+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" .
}