@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY
> .
@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:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_head
{
this:
np:hasAssertion
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_assertion
;
np:hasProvenance
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_provenance
;
np:hasPublicationInfo
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_assertion
a
np:Assertion
.
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_provenance
a
np:Provenance
.
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGNb351a8003699e528b7e442f4b06bc8b8
sio:SIO_000628
miriam-gene:351
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_provenance
{
dgn-np:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_assertion
dcterms:description
"[Inclusion body myositis, the most common muscle disorder in the elderly, is partly characterized by abnormal expression of amyloid precursor protein (APP) and intracellular accumulation of its proteolytic fragments collectively known as β-amyloid.]. 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:22518836
;
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:NP391478.RARKLFhEJVOI1sW3Lad0zslHIwq_fxMt-yETU4IgLIvHY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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: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" .
}