@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0
> .
@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:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_head
{
this:
np:hasAssertion
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_assertion
;
np:hasProvenance
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_provenance
;
np:hasPublicationInfo
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_assertion
a
np:Assertion
.
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_provenance
a
np:Provenance
.
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0027066
a
ncit:C7057
.
dgn-gda:DGN7f3de453c1e155eb02df93ae29d99a48
sio:SIO_000628
miriam-gene:348
,
lld:C0027066
;
a
sio:SIO_001121
.
}
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_provenance
{
dgn-np:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_assertion
dcterms:description
"[Because the decline in mental ability as well as the development of myoclonus and extrapyramidal signs are consistent manifestations of disease progression, our results imply that APOE epsilon4 is associated with a less aggressive form of AD.]. 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:9153523
;
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:NP429238.RAX8ef5gH_02kRNuRjnQcsQf6b2r1qMD-lenAioW6oDF0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}