@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw
> .
@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:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_head
{
this:
np:hasAssertion
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_assertion
;
np:hasProvenance
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_assertion
a
np:Assertion
.
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_provenance
a
np:Provenance
.
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNbaceb22db6652411eafde591c6801824
sio:SIO_000628
miriam-gene:348
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_provenance
{
dgn-np:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_assertion
dcterms:description
"[Although samples enriched for APOE ε4 carriers in AD or MCI clinical trials showed slightly more cognitive impairment and greater decline using the number APOE ε4 alleles as an inclusion criterion most likely would not result in more efficient trials, and trials would take longer because fewer patients would be available.]. 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:23712001
;
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:NP1081081.RAeiloVyQ2D383v4PGdKEIpLlR6jQ3Rcbw8CB__MxSomw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:56+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" .
}