@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE
> .
@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:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_head
{
this:
np:hasAssertion
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_assertion
;
np:hasProvenance
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_provenance
;
np:hasPublicationInfo
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_assertion
a
np:Assertion
.
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_provenance
a
np:Provenance
.
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_assertion
{
miriam-gene:2030
a
ncit:C16612
.
lld:C0019196
a
ncit:C7057
.
dgn-gda:DGN92867a24a621f166452a836a66c071b1
sio:SIO_000628
miriam-gene:2030
,
lld:C0019196
;
a
sio:SIO_001121
.
}
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_provenance
{
dgn-np:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_assertion
dcterms:description
"[Patients (n=169) chronically infected with the hepatitis C virus genotype 1, treated with standard doses of pegylated interferon-α and weight-based doses of ribavirin for up to 48 weeks, were genotyped for 21 variants in nucleoside transporter genes SLC28A2, SLC28A3, SLC29A1, and SLC29A2, selected to include reported functional variants and to span the complete gene loci.]. 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:21346688
;
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:NP399358.RAXWiwWjf1G0DkZ94nZC7m9E7XSltOtByv_2abXg21WTE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}