@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU
> .
@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:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_head
{
this:
np:hasAssertion
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_assertion
;
np:hasProvenance
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_provenance
;
np:hasPublicationInfo
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_assertion
a
np:Assertion
.
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_provenance
a
np:Provenance
.
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_assertion
{
miriam-gene:3627
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGN0e62b7c386155cc1d399013b85a7ce32
sio:SIO_000628
miriam-gene:3627
,
lld:C0524910
;
a
sio:SIO_001121
.
}
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_provenance
{
dgn-np:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_assertion
dcterms:description
"[High baseline levels of IP-10 predict a slower first phase decline in HCV RNA and a poor outcome following interferon/ribavirin therapy in patients with chronic hepatitis C. Several recent studies report that single nucleotide polymorphisms (SNPs) adjacent to IL28B predict spontaneous resolution of HCV infection and outcome of treatment among HCV genotype 1 infected patients.]. 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:21390311
;
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:NP205640.RAigZ8rwZo4YLaTzYTiIiv6vIE-qPVHW35aY5QE8RIctU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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" .
}