@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg
> .
@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:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_head
{
this:
np:hasAssertion
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_assertion
;
np:hasProvenance
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_provenance
;
np:hasPublicationInfo
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_assertion
a
np:Assertion
.
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_provenance
a
np:Provenance
.
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0022104
a
ncit:C7057
.
dgn-gda:DGN592486a9b68cc54f046dd043e3ba98de
sio:SIO_000628
miriam-gene:348
,
lld:C0022104
;
a
sio:SIO_001121
.
}
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_provenance
{
dgn-np:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_assertion
dcterms:description
"[The linkage to chromosome 19 was well explained by APOE in the whole sample as well as in the UK and USA subsamples, as identity by descent (IBD) increased with the number of epsilon4 alleles in ASPs.]. 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:18161859
;
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:NP781523.RA4McNQCazV2URPq0qgCFiew97ESq25YqJ7gsHm1X7iXg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}