@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_head
{
this:
np:hasAssertion
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_assertion
;
np:hasProvenance
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_provenance
;
np:hasPublicationInfo
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_assertion
a
np:Assertion
.
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_provenance
a
np:Provenance
.
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0018995
a
ncit:C7057
.
dgn-gda:DGN8d4e7592a882a6139c5b8cef2839ad9a
sio:SIO_000628
miriam-gene:3077
,
lld:C0018995
;
a
sio:SIO_001122
.
}
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_provenance
{
dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_assertion
dcterms:description
"[study of H63D homozygotes supports the conclusion that this genotype must be taken into account, because it confers an increased risk of iron overload and genetic susceptibility to developing hereditary hemochromatosis or to aggravating other diseases ]. 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:16364490
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:24+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}