@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk
> .
@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:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_head
{
this:
np:hasAssertion
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_assertion
;
np:hasProvenance
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_provenance
;
np:hasPublicationInfo
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_assertion
a
np:Assertion
.
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_provenance
a
np:Provenance
.
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_assertion
{
miriam-gene:3439
a
ncit:C16612
.
lld:C0015695
a
ncit:C7057
.
dgn-gda:DGNb45d09f2ab09dab9b6b6c27a572bc6ab
sio:SIO_000628
miriam-gene:3439
,
lld:C0015695
;
a
sio:SIO_001121
.
}
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_provenance
{
dgn-np:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_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:NP563807.RAdAQTvx-8exlzlXu3ZEbkZpiiwhghahNzkAw97tJVRlk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}