@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok
> .
@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:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_head
{
this:
np:hasAssertion
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_assertion
;
np:hasProvenance
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_provenance
;
np:hasPublicationInfo
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_assertion
a
np:Assertion
.
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_provenance
a
np:Provenance
.
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_assertion
{
miriam-gene:79879
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN7fdddf436bb8176009d6a574dcd6f8b7
sio:SIO_000628
miriam-gene:79879
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_provenance
{
dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_assertion
dcterms:description
"[In addition to known candidate genes, APOE, TOMM40, and one hypothetical gene LOC100129500 partially overlapping APOE; one novel gene, EPC2, and several other interesting genes were associated with CSF biomarkers that are related to AD. These findings, especially the new EPC2 results, require replication in independent cohorts.]. 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:21123754
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:47+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" .
}