@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU
> .
@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:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_head
{
this:
np:hasAssertion
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_assertion
;
np:hasProvenance
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_provenance
;
np:hasPublicationInfo
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_assertion
a
np:Assertion
.
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_provenance
a
np:Provenance
.
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C3241937
a
ncit:C7057
.
dgn-gda:DGN083d76f5717e431f4d4a4461cedd4617
sio:SIO_000628
miriam-gene:3630
,
lld:C3241937
;
a
sio:SIO_001121
.
}
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_provenance
{
dgn-np:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_assertion
dcterms:description
"[Serum ferritin concentrations were measured in 86 patients with histopathologically verified NAFLD (24 with steatosis and 62 with NASH) and 20 control subjects, they were tested for HFE gene mutations and their insulin resistance was measured.]. 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:19267193
;
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:NP306361.RAmwmT9VbPNS1LP9vi7RJ6qMNC2RGXEra8HffBsCVFiIU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}