@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY
> .
@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:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_head
{
this:
np:hasAssertion
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_assertion
;
np:hasProvenance
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_provenance
;
np:hasPublicationInfo
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_assertion
a
np:Assertion
.
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_provenance
a
np:Provenance
.
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_assertion
{
miriam-gene:3115
a
ncit:C16612
.
lld:C0019163
a
ncit:C7057
.
dgn-gda:DGNade7955771cb6af82abc2e29122de1af
sio:SIO_000628
miriam-gene:3115
,
lld:C0019163
;
a
sio:SIO_001121
.
}
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_provenance
{
dgn-np:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_assertion
dcterms:description
"[Two HLA-DP gene variants (rs3077 and rs9277535) were analyzed for associations with persistent HBV infection and with different clinical outcomes, i.e., inactive HBsAg carrier status versus progressive chronic HBV (CHB) infection in Caucasian patients (n = 201) and HBsAg negative controls (n = 235).]. 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:22448225
;
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:NP479393.RAmyOaSfTcSSg-t4efjFhDJ0BIbWrbgaq5B0t2VdSB1aY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}