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http://rdf.disgenet.org/nanopublications.trig#NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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http://linkedlifedata.com/resource/umls/id/
> .
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http://identifiers.org/ncbigene/
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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dgn-np:NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo130_assertion
a
np:Assertion
.
dgn-np:NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo130_provenance
a
np:Provenance
.
dgn-np:NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo130_assertion
{
miriam-gene:1292
a
ncit:C16612
.
lld:C1852502
a
ncit:C7057
.
dgn-gda:DGNd9e8c38fdf37d37e872dd5beba7c0ae3
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miriam-gene:1292
,
lld:C1852502
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.
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dgn-np:NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo130_provenance
{
dgn-np:NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo130_assertion
dcterms:description
"[Motor and sensory nerve conduction velocities (NCVs) and needle electromyography (EMG) results were reviewed in 26 children with different types of congenital muscular dystrophy (CMD), including patients with mutations in the genes LAMA2, FKRP, and COL6A2.]. 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:14755496
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP782098.RAHrnSNbRifTIpoXODLd1SXHfg4NLHG7oWF0S1yrVUNlo130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
dgn-void:disgenetrdf
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> , <
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> ;
pav:createdBy
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pav:version
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