@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU
> .
@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:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_head
{
this:
np:hasAssertion
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_assertion
;
np:hasProvenance
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_provenance
;
np:hasPublicationInfo
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_assertion
a
np:Assertion
.
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_provenance
a
np:Provenance
.
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_assertion
{
miriam-gene:30816
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGN189fd9fe75c5d84c7784b6a20fb15957
sio:SIO_000628
miriam-gene:30816
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_provenance
{
dgn-np:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_assertion
dcterms:description
"[This finding suggests that nucleotide mutations in the envelope region of the viral genome may be responsible for the recurrent hepatic injury attributed to recurrence of viremia in patients with hepatitis C. From these aspects, the serial divergence of the virus genome in infected individuals, especially in the region encoding the viral envelope protein, may possibly play an important role in developing chronic infection of hepatitis C virus.]. 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:1330930
;
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:NP617752.RAqR3UELXbc3TVcunxCAy0Rir9tA3DhIqCf5sdv9807bU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}