@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion
a
np:Assertion
.
dgn-np:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance
a
np:Provenance
.
dgn-np:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C0001973
a
ncit:C7057
.
dgn-gda:DGN2220fea537e87e1f73367778ce6c7f63
sio:SIO_000628
miriam-gene:551
,
lld:C0001973
;
a
sio:SIO_001121
.
}
dgn-np:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_provenance
{
dgn-np:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_assertion
dcterms:description
"[Genotypes were available for 40 SNPs across the ADH genes cluster and 24 SNPs across the two ALDH genes in four diverse samples that included cases (lifetime AD) and controls (no Axis 1 disorders).]. 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:21083667
;
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:NP852978.RA_mZZrHLzSl1nAUeUdTHEnzANL9KoMuFK5UfL_cDV13I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:11+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" .
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pav:version
"v4.0.0" .
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