@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc
> .
@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:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_head
{
this:
np:hasAssertion
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_assertion
;
np:hasProvenance
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_provenance
;
np:hasPublicationInfo
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_assertion
a
np:Assertion
.
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_provenance
a
np:Provenance
.
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_assertion
{
miriam-gene:3704
a
ncit:C16612
.
lld:C0002878
a
ncit:C7057
.
dgn-gda:DGN77dab7f5b95c97d2ebc576cb495e695c
sio:SIO_000628
miriam-gene:3704
,
lld:C0002878
;
a
sio:SIO_001121
.
}
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_provenance
{
dgn-np:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_assertion
dcterms:description
"[Recently, genome-wide association studies (GWAS) in patients with chronic hepatitis C virus (HCV) infection have identified two functional single nucleotide polymorphisms (SNPs) in the inosine triphosphatase (ITPA) gene, that are associated strongly and independently with hemolytic anemia in patients exposed to pegylated-interferon (Peg-IFN) plus ribavirin (RBV) combined therapy.]. 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:23201294
;
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:NP448158.RAXEaKvM-eJdEk2Yc_LYbT3739BY8TGz9_phKy0HFEYyc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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" .
}