@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0
> .
@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:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_head
{
this:
np:hasAssertion
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_assertion
;
np:hasProvenance
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_provenance
;
np:hasPublicationInfo
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_assertion
a
np:Assertion
.
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_provenance
a
np:Provenance
.
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_assertion
{
miriam-gene:6648
a
ncit:C16612
.
lld:C0878544
a
ncit:C7057
.
dgn-gda:DGN07df02b68190697323137de9df21aa81
sio:SIO_000628
miriam-gene:6648
,
lld:C0878544
;
a
sio:SIO_001122
.
}
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_provenance
{
dgn-np:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_assertion
dcterms:description
"[In patients with hereditary haemochromatosis, the MnSOD genotype affects the risk of cardiomyopathy related to iron overload and possibly to other known and unknown risk factors and could represent an iron toxicity modifier 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:15591282
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP51215.RAnC4QlxtygH7qPiYoNfG_bVKotdfSRTCQRZx92Ywlvj0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}