@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08
> .
@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:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_head
{
this:
np:hasAssertion
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_assertion
;
np:hasProvenance
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_provenance
;
np:hasPublicationInfo
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_assertion
a
np:Assertion
.
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_provenance
a
np:Provenance
.
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_assertion
{
miriam-gene:3447
a
ncit:C16612
.
lld:C2711227
a
ncit:C7057
.
dgn-gda:DGNe224c8f8ace6bd9b550e2d011c3d16be
sio:SIO_000628
miriam-gene:3447
,
lld:C2711227
;
a
sio:SIO_001121
.
}
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_provenance
{
dgn-np:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_assertion
dcterms:description
"[With the exception of two patients infected with genotype 3a, the rate of liver steatosis was found to be high and did not change after IFN treatment in HD patients with CHC.]. 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:16990211
;
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:NP379231.RAXSpUD6Kn5qCngTIwP_rw87-VCb7fa7hGG6PmvT4ok08130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:44+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" .
}