@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM
> .
@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:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_head
{
this:
np:hasAssertion
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_assertion
;
np:hasProvenance
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_provenance
;
np:hasPublicationInfo
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_assertion
a
np:Assertion
.
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_provenance
a
np:Provenance
.
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_assertion
{
miriam-gene:57126
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN44a5726581325e707d6b9a99a99de448
sio:SIO_000628
miriam-gene:57126
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_provenance
{
dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_assertion
dcterms:description
"[This sequence, together with the localization of its gene on chromosome 21, suggests that the cerebral amyloid deposited in Alzheimer's disease and aged Down's syndrome is caused by aberrant catabolism of a cell-surface receptor.]. 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:2881207
;
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:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}