@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo
> .
@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:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_head
{
this:
np:hasAssertion
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_assertion
;
np:hasProvenance
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_provenance
;
np:hasPublicationInfo
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_assertion
a
np:Assertion
.
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_provenance
a
np:Provenance
.
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN4b98f10dab64bcb9a26a86a2c255e8d4
sio:SIO_000628
miriam-gene:3077
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_provenance
{
dgn-np:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_assertion
dcterms:description
"[Hereditary Hemochromatosis (HH) is an iron overload syndrome caused by increased duodenal iron absorption, which leads to excessive iron deposition in parenchymal cells of the liver and mayor organs, causing cirrhosis, diabetes, cardiac failure, endocrine complications and arthritis.]. 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:19656448
;
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:NP427669.RA9z53sj7IihUyKv9GhX9eTG6cSIoyh40ZEOdC6yutYAo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}