@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU
> .
@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:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_head
{
this:
np:hasAssertion
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_assertion
;
np:hasProvenance
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_provenance
;
np:hasPublicationInfo
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_assertion
a
np:Assertion
.
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_provenance
a
np:Provenance
.
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_assertion
{
miriam-gene:26585
a
ncit:C16612
.
lld:C0238190
a
ncit:C7057
.
dgn-gda:DGNe9011234c09c313858f31fb37548dfc4
sio:SIO_000628
miriam-gene:26585
,
lld:C0238190
;
a
sio:SIO_001121
.
}
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_provenance
{
dgn-np:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_assertion
dcterms:description
"[There are certain similarities between IBM and DRM: midlife or late-onset clinical symptoms, apparently of both sporadic and genetic background, morphologically autophagocytosis by vacuole formation, which is frequent in IBM though rare in DRM, and presence of tubulofilamentous aggregates, which is almost regular in IBM but scantily found in DRM as beta-amyloid components have been identified as accruing proteins, both in IBM and DRM.]. 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:21528768
;
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:NP392781.RAx6nKj3m660LbzgkdgXtF06fq60VtsqMuYREpbuktsPU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}