@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE
> .
@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:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_head
{
this:
np:hasAssertion
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_assertion
;
np:hasProvenance
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_provenance
;
np:hasPublicationInfo
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_assertion
a
np:Assertion
.
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_provenance
a
np:Provenance
.
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0086181
a
ncit:C7057
.
dgn-gda:DGN373ac8ecb632e9fe1eb808498d432a6e
sio:SIO_000628
miriam-gene:2837
,
lld:C0086181
;
a
sio:SIO_001121
.
}
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_provenance
{
dgn-np:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_assertion
dcterms:description
"[The genotype of hepatitis C virus (HCV) of 172 HCV-RNA positive serum specimens taken from patients with chronic liver diseases, thalassaemia major, chronic renal failure (CRF), haemophilia and intravenous drug abusers (IVDA) was determined by analysis of the amplified 5'UTR region by genotype-specific oligonucleotide probes and restriction fragment length polymorphism (RFLP).]. 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:9744672
;
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:NP939571.RAGK_aQbQ4PaE2lBGkpcAU9eX0sazn_TzWSXuLm4dFeIE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}