@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ
> .
@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:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_head
{
this:
np:hasAssertion
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_assertion
;
np:hasProvenance
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_assertion
a
np:Assertion
.
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_provenance
a
np:Provenance
.
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_assertion
{
miriam-gene:10020
a
ncit:C16612
.
lld:C0004093
a
ncit:C7057
.
dgn-gda:DGN9ca6f9428e22a3cfadd453163e9e2d5e
sio:SIO_000628
miriam-gene:10020
,
lld:C0004093
;
a
sio:SIO_001121
.
}
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_provenance
{
dgn-np:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_assertion
dcterms:description
"[However, the two patients demonstrated different patterns of disease progression: one had slow disease progression with a typical feature of DMRV (that is, weakness beginning in the distal leg muscles, typically anterior tibialis, with the quadriceps remaining relatively unaffected), and the other had rapid disease progression with an atypical presentation of DMRV.]. 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:15834044
;
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:NP561057.RAGeySiraDmUZnFXurm6e3KnI_eLXzcY4e2CQnTEGeNWQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}