@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE
> .
@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:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_head
{
this:
np:hasAssertion
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_assertion
;
np:hasProvenance
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_assertion
a
np:Assertion
.
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_provenance
a
np:Provenance
.
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN1601cd214a881fb953f35af4a7aac681
sio:SIO_000628
miriam-gene:348
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_provenance
{
dgn-np:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_assertion
dcterms:description
"[These findings suggest that small HC limits educational attainment only among individuals who have greater risk of AD owing to their APOE genotype or who are destined to develop this illness later in life.]. 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:18580587
;
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:NP678802.RADaPT5wta-8uqQh2gRuitpVS8uFGJlX54hENOUJeVQgE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:53+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: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" .
}