@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM
> .
@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:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_head
{
this:
np:hasAssertion
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_assertion
;
np:hasProvenance
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_provenance
;
np:hasPublicationInfo
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_assertion
a
np:Assertion
.
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_provenance
a
np:Provenance
.
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_assertion
{
miriam-gene:3447
a
ncit:C16612
.
lld:C0019189
a
ncit:C7057
.
dgn-gda:DGN1350cc63c438a1009828746fb1be4b85
sio:SIO_000628
miriam-gene:3447
,
lld:C0019189
;
a
sio:SIO_001121
.
}
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_provenance
{
dgn-np:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_assertion
dcterms:description
"[Interleukin-28B (IL28B) single nucleotide polymorphism (SNP) influences viral response (VR) to interferon (IFN) therapy in patients with hepatitis C. We studied the relationship between VR and the IL28B polymorphism (rs8099917) in patients on long-term pegylated IFN plus ribavirin (PEGIFN/RBV) therapy for recurrent hepatitis C after living-donor liver transplantation (LDLT).]. 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:22432893
;
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:NP412446.RALzxPO6MZOxq8TiGTxJ2mDGlcxb6hUsj-BTf3m8GUAEM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}