@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY
> .
@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:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_head
{
this:
np:hasAssertion
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_assertion
;
np:hasProvenance
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_provenance
;
np:hasPublicationInfo
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_assertion
a
np:Assertion
.
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_provenance
a
np:Provenance
.
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C3241937
a
ncit:C7057
.
dgn-gda:DGNc4a4c7b14522fdd0628d88c3ecc04ff6
sio:SIO_000628
miriam-gene:3077
,
lld:C3241937
;
a
sio:SIO_001121
.
}
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_provenance
{
dgn-np:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_assertion
dcterms:description
"[Serum ferritin concentration, liver function test results, and fibrosis grade were more elevated in patients with steatosis and NASH than in others, but LIC and allelic frequencies of HFE mutations were similar.]. 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:10535879
;
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:NP848825.RA9dSlPQfrw4FFEsu8M-v8etEFh7OEoB1uGsM4cSUBUFY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}