@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_head
{
this:
np:hasAssertion
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_assertion
;
np:hasProvenance
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_provenance
;
np:hasPublicationInfo
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_assertion
a
np:Assertion
.
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_provenance
a
np:Provenance
.
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_assertion
{
miriam-gene:217
a
ncit:C16612
.
lld:C0001973
a
ncit:C7057
.
dgn-gda:DGNbf8957df855a500cc044be133ba57730
sio:SIO_000628
miriam-gene:217
,
lld:C0001973
;
a
sio:SIO_001121
.
}
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_provenance
{
dgn-np:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_assertion
dcterms:description
"[Their results actually show there is a pleiotropic effect associated with the mutation ALDH2(() 487Lys allele that is as deleterious as the risk of alcoholism for which it offers protection, and thus there is no net benefit from having the mutation.]. 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:17103300
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP579277.RA0j4MAJxZxaUGOqt7jX3_W8SiEytG_yjQGP9CEtKbOGM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:07+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}