@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ
> .
@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:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_head
{
this:
np:hasAssertion
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_assertion
;
np:hasProvenance
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_assertion
a
np:Assertion
.
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_provenance
a
np:Provenance
.
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_assertion
{
miriam-gene:125
a
ncit:C16612
.
lld:C0001973
a
ncit:C7057
.
dgn-gda:DGN3ab98e8434b6119d5bec144b01242929
sio:SIO_000628
miriam-gene:125
,
lld:C0001973
;
a
sio:SIO_001121
.
}
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_provenance
{
dgn-np:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_assertion
dcterms:description
"[Genetic variation at two polymorphic alcohol dehydrogenase loci, ADH2 and ADH3, and at the polymorphic mitochondrial aldehyde dehydrogenase locus, ALDH2, may influence the risk of developing alcoholism by modulating the rate of elimination of ethanol and the rate of formation and elimination of acetaldehyde.]. 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:7943668
;
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:NP177741.RAeiomLEls9gH0Dy9mttSsw4oXX3VJoSfyDRkwSs4MLXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}