@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k
> .
@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:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_head
{
this:
np:hasAssertion
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_assertion
;
np:hasProvenance
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_provenance
;
np:hasPublicationInfo
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_assertion
a
np:Assertion
.
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_provenance
a
np:Provenance
.
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_assertion
{
miriam-gene:3447
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN03fc3dc029a39a31bf8f9a1e054a30b3
sio:SIO_000628
miriam-gene:3447
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_provenance
{
dgn-np:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_assertion
dcterms:description
"[Recent reports show that R70Q and L/C91M amino acid substitutions in the core from different hepatitis C virus (HCV) genotypes have been associated with variable responses to interferon (IFN) and ribavirin (RBV) therapy, as well to an increase of hepatocellular carcinoma (HCC) risk, liver steatosis and insulin resistance (IR).]. 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:22995142
;
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:NP280786.RAuUjwKTdUntBHqqvWi5jrKsCuVi_TrLvrq0lJhi9KJ5k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}