@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c
> .
@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:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_head
{
this:
np:hasAssertion
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_assertion
;
np:hasProvenance
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_provenance
;
np:hasPublicationInfo
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_assertion
a
np:Assertion
.
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_provenance
a
np:Provenance
.
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_assertion
{
miriam-gene:2694
a
ncit:C16612
.
lld:C2711227
a
ncit:C7057
.
dgn-gda:DGNdba74c5c37c745d6233f201af026db41
sio:SIO_000628
miriam-gene:2694
,
lld:C2711227
;
a
sio:SIO_001121
.
}
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_provenance
{
dgn-np:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_assertion
dcterms:description
"[The aim of this work was to assess the frequency of LS, its relationship with host and viral factors and to what extent it can influence the response to antiviral combination therapy with pegylated interferon (INF)+ribavirin in a group of patients with CHC from a single center.]. 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:17032413
;
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:NP799949.RAH4AInFco4cSF_ynG6BdxMpxQkyRTt0Sag0SMV2dsd9c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}