@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA
> .
@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:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_head
{
this:
np:hasAssertion
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_assertion
;
np:hasProvenance
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_provenance
;
np:hasPublicationInfo
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_assertion
a
np:Assertion
.
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_provenance
a
np:Provenance
.
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGN46f5b2ba985c781971985af7a2d58f04
sio:SIO_000628
miriam-gene:3077
,
lld:C0524910
;
a
sio:SIO_001121
.
}
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_provenance
{
dgn-np:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_assertion
dcterms:description
"[The aim of this study was to assess occurrence of iron overload in relation to polymorphism of the HFE and the influence of both these factors on efficacy of antiviral treatment with pegylated interferon and ribavirin in 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:20190684
;
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:NP213832.RAUpMZyf3hnSqDp1-RmKsWFW1c3i3hR6h8k-Uq_cm7cuA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:58+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" .
}