@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ
> .
@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:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_head
{
this:
np:hasAssertion
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_assertion
;
np:hasProvenance
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_assertion
a
np:Assertion
.
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_provenance
a
np:Provenance
.
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_assertion
{
miriam-gene:3439
a
ncit:C16612
.
lld:C0002878
a
ncit:C7057
.
dgn-gda:DGN65d12bb1046db17250b16fb00fb441b8
sio:SIO_000628
miriam-gene:3439
,
lld:C0002878
;
a
sio:SIO_001121
.
}
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_provenance
{
dgn-np:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_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:NP426090.RAyVFEPZJyiGxJHu47mB0dIZ-_U-n4CjpDdhku8zYaFYQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}