@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc
> .
@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:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_head
{
this:
np:hasAssertion
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_assertion
;
np:hasProvenance
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_provenance
;
np:hasPublicationInfo
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_assertion
a
np:Assertion
.
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_provenance
a
np:Provenance
.
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_assertion
{
miriam-gene:126
a
ncit:C16612
.
lld:C0001973
a
ncit:C7057
.
dgn-gda:DGN2886399db109d9a0a9c60b41e7f56c64
sio:SIO_000628
miriam-gene:126
,
lld:C0001973
;
a
sio:SIO_001121
.
}
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_provenance
{
dgn-np:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_assertion
dcterms:description
"[The alcoholics had significantly lower frequencies of the ADH2*2, ADH3*1, and ALDH2*2 alleles than did the nonalcoholics, suggesting that genetic variation in both ADH and ALDH, by modulating the rate of metabolism of ethanol and acetaldehyde, influences drinking behavior and the risk of developing alcoholism.]. 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:2014795
;
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:NP335380.RADDjWv-J7Tq3MvcHM-SF2LsElhEhMSWYzleL_KscMghc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}