@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g
> .
@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:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_head
{
this:
np:hasAssertion
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_assertion
;
np:hasProvenance
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_assertion
a
np:Assertion
.
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_provenance
a
np:Provenance
.
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C1270972
a
ncit:C7057
.
dgn-gda:DGN1e95f8f8e2103a510312a3d4a7aad0fa
sio:SIO_000628
miriam-gene:348
,
lld:C1270972
;
a
sio:SIO_001121
.
}
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_provenance
{
dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_assertion
dcterms:description
"[To determine whether memory loss is detectable before the symptomatic presentation of mild cognitive impairment (MCI) in those at greater genetic risk for Alzheimer disease (AD) based upon presence or absence of the e4 allele of APOE.]. 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:15184602
;
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:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_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" .
}