@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA
> .
@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:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_head
{
this:
np:hasAssertion
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_assertion
;
np:hasProvenance
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_provenance
;
np:hasPublicationInfo
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_assertion
a
np:Assertion
.
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_provenance
a
np:Provenance
.
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_assertion
{
miriam-gene:3658
a
ncit:C16612
.
lld:C0018995
a
ncit:C7057
.
dgn-gda:DGN0394e40fe36cfd031a8354ba8adb611e
sio:SIO_000628
miriam-gene:3658
,
lld:C0018995
;
a
sio:SIO_001122
.
}
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_provenance
{
dgn-np:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_assertion
dcterms:description
"[gene coding and flanking regions were sequenced and examined for mutations that might modulate the iron burden of individuals harboring the common mutant hemochromatosis HFE genotype or cause hemochromatosis independent of mutations in the HFE gene ]. 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:11783942
;
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:NP148067.RABSqZmXkuxFQMBYCUt2RCzip1Iw1tQQWIChusTLhrMtA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:17+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" .
}