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http://rdf.disgenet.org/nanopublications.trig#NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_assertion
a
np:Assertion
.
dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_provenance
a
np:Provenance
.
dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:6046
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN5fdac2a8157ac763cea670dadaeb5c17
sio:SIO_000628
miriam-gene:6046
,
lld:C0026848
;
a
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.
}
dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_provenance
{
dgn-np:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_assertion
dcterms:description
"[Serum creatine-kinase (CK) isoenzyme MB was measured in 53 patients affected by different types of myopathies (20 with Duchenne muscular dystrophy (DMD), eight with the Becker form (BMD), ten with the limb-girdle form (LGMD), six with the facioscapulohumeral form (FSH), and nine affected by polymyositis and in 21 normal control subjects).]. 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:4050853
;
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:NP897490.RA9M1D-ilwXmbrTPPT431EwpCKotQ7WHZIQ0sS0647SgM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:11+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
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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