@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI
> .
@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:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_head
{
this:
np:hasAssertion
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_assertion
;
np:hasProvenance
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_provenance
;
np:hasPublicationInfo
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_assertion
a
np:Assertion
.
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_provenance
a
np:Provenance
.
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGN390606adeb7472bf404c6dc7264fd443
sio:SIO_000628
miriam-gene:3077
,
lld:C0524910
;
a
sio:SIO_001122
.
}
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_provenance
{
dgn-np:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_assertion
dcterms:description
"[The presence of HFE mutations is independently associated with iron loading and advanced fibrosis in patients with compensated liver disease from chronic hepatitis C, especially after controlling for duration of disease.]. 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:12557137
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP138422.RA7VlJHQgLaQddX07zvNn1O8AW0AZvwPmqrZ3HLvYFcaI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:12+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" .
}