@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU
> .
@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:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_head
{
this:
np:hasAssertion
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_assertion
;
np:hasProvenance
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_assertion
a
np:Assertion
.
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_provenance
a
np:Provenance
.
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_assertion
{
miriam-gene:217
a
ncit:C16612
.
lld:C0023896
a
ncit:C7057
.
dgn-gda:DGNadb006e65ec9915f6a13a44cc40cd5ec
sio:SIO_000628
miriam-gene:217
,
lld:C0023896
;
a
sio:SIO_001121
.
}
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_provenance
{
dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_assertion
dcterms:description
"[These results confirmed the previous observation that the incidence of ALDH2 deficiency is much lower in alcoholic liver disease patients than in the general population, and suggested that most of the ALDH2 deficient patients with alcoholic liver disease are heterozygous for the normal and mutant ALDH2 genes.]. 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:1916152
;
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:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}