@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ
> .
@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:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_head
{
this:
np:hasAssertion
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_assertion
;
np:hasProvenance
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_assertion
a
np:Assertion
.
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_provenance
a
np:Provenance
.
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0042769
a
ncit:C7057
.
dgn-gda:DGN2de00a5c8e544c829a3f898ce5a2147b
sio:SIO_000628
miriam-gene:3126
,
lld:C0042769
;
a
sio:SIO_001121
.
}
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_provenance
{
dgn-np:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_assertion
dcterms:description
"[To demonstrate the association of HLA allele polymorphism in combination with HBV subgenotypes with the outcome of HBV infection in Northeastern Han Chinese population, a total of 230 HBV-infected individuals (Infection group) were compared to 210 random selected controls (Control group) who are negative for HBV infection for their HLA alleles frequency as well as the associations with the virus infection, clearance and persistence in combination with HBV subgenotypes.]. 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:22056847
;
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:NP560676.RAnzGk7ngElayp7_Dw4ZHRbVhh8uXTzwiNR_MEGDbw6rQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}