@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A
> .
@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/v3.0.0/void/
> .
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_head
{
this:
np:hasAssertion
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_assertion
;
np:hasProvenance
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_assertion
a
np:Assertion
.
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_provenance
a
np:Provenance
.
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0015695
a
ncit:C7057
.
dgn-gda:DGN5cd5e4edb8bada7ebed1415e6c8ac025
sio:SIO_000628
miriam-gene:3077
,
lld:C0015695
;
a
sio:SIO_001122
.
}
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_provenance
{
dgn-np:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_assertion
dcterms:description
"[The presence of H63D mutations was an independent factor associated with NAFLD and elevated TS. Therefore, the H63D mutation may increase susceptibility to NAFLD probably associated with peripheral iron overload, especially in males.]. 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:20216079
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP137369.RAZFUlBKXn_rZ_cISb36CC6UNvIPDT1MasqPV0HUSQh5A130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:57+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}