@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg
> .
@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:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_head
{
this:
np:hasAssertion
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_assertion
;
np:hasProvenance
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_provenance
;
np:hasPublicationInfo
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_assertion
a
np:Assertion
.
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_provenance
a
np:Provenance
.
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_assertion
{
miriam-gene:611
a
ncit:C16612
.
lld:C0524909
a
ncit:C7057
.
dgn-gda:DGN0c3e3e501ccd21c14fbd074072ef0d9b
sio:SIO_000628
miriam-gene:611
,
lld:C0524909
;
a
sio:SIO_001121
.
}
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_provenance
{
dgn-np:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_assertion
dcterms:description
"[For this study HBV DNA was amplified and then sequenced to show the presence of the basal core promoter (BCP) mutations in the serum from 57 patients with chronic hepatitis B.]. 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:23080492
;
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:NP522168.RAnMicKstDZiK3b4SeEIakLHBQTE2P51myxX8uxkcVmpg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}