@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA
> .
@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:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_head
{
this:
np:hasAssertion
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_assertion
;
np:hasProvenance
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_provenance
;
np:hasPublicationInfo
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_assertion
a
np:Assertion
.
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_provenance
a
np:Provenance
.
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_assertion
{
miriam-gene:28509
a
ncit:C16612
.
lld:C0151786
a
ncit:C7057
.
dgn-gda:DGNfbd150a4b037b7b300492925937f837e
sio:SIO_000628
miriam-gene:28509
,
lld:C0151786
;
a
sio:SIO_001121
.
}
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_provenance
{
dgn-np:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_assertion
dcterms:description
"[Myotonic dystrophy type 1 (DM1), one of the most common forms of inherited neuromuscular disorders in the adult, is characterized by progressive muscle weakness and wasting leading to distal muscle atrophy whereas proximal muscles of the same patients are spared during the early phase of the disease.]. 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:19207265
;
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:NP830587.RAqLzFP24SgJw91t5y02UDZR-1GWTZnWB8nuhNFTWcUAA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}