@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww
> .
@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:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_head
{
this:
np:hasAssertion
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_assertion
;
np:hasProvenance
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_provenance
;
np:hasPublicationInfo
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_assertion
a
np:Assertion
.
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_provenance
a
np:Provenance
.
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_assertion
{
miriam-gene:217
a
ncit:C16612
.
lld:C0029445
a
ncit:C7057
.
dgn-gda:DGN18d9357a55c7e3616f4c14e846b9d2c0
sio:SIO_000628
miriam-gene:217
,
lld:C0029445
;
a
sio:SIO_001122
.
}
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_provenance
{
dgn-np:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_assertion
dcterms:description
"[The reason for the insignificant multivariate OR of ALDH2(1/1) may be due to the strong confounding of alcohol consumption on the association between ALDH2 genotype and ION. For females, the small sample size made it impossible to produce any meaningful univariate analysis.]. 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:14768474
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48688.RAOLuji2vcFk7PKkz9kf5Mnge4ov6gBqaubEzlmicyUww130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}