@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk
> .
@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:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_head
{
this:
np:hasAssertion
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_assertion
;
np:hasProvenance
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_provenance
;
np:hasPublicationInfo
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_assertion
a
np:Assertion
.
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_provenance
a
np:Provenance
.
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0239946
a
ncit:C7057
.
dgn-gda:DGN1a772ef4acd9805a4d327fa5f0415370
sio:SIO_000628
miriam-gene:3077
,
lld:C0239946
;
a
sio:SIO_001121
.
}
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_provenance
{
dgn-np:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_assertion
dcterms:description
"[It is less well established that the prevalence of the HFE mutations is increased in alcoholic liver disease and in chronic viral hepatitis, but in both conditions, patients harboring one of these mutations, especially C282Y, are more likely to have advanced hepatic fibrosis or cirrhosis.]. 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:10980924
;
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:NP402780.RARyb9RYbwuYEMh8OLJjPxfp1TZmWNKQaJKhHn5iDTDHk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}