@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI> .
@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:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_head {
  this: np:hasAssertion dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_assertion ;
    np:hasProvenance dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_provenance ;
    np:hasPublicationInfo dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_assertion a np:Assertion .
  dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_provenance a np:Provenance .
  dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_assertion {
  miriam-gene:8291 a ncit:C16612 .
  lld:C0030552 a ncit:C7057 .
  dgn-gda:DGNb59cfbc45b2a1569061f40d0a77ea1f2 sio:SIO_000628 miriam-gene:8291 , lld:C0030552 ;
    a sio:SIO_001121 .
}
dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_provenance {
  dgn-np:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_assertion dcterms:description "[In the early stages of disease these patients may clinically show only proximal lower limb-girdle muscle weakness; however, the use of muscle imaging techniques were very important, always detecting in these patients also distal lower limb muscle involvement, so that the pattern of muscle involvement found in dysferlin deficiency may not strictly conform to the definition of limb-girdle muscular dystrophy.]. 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:11166162 ;
    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:NP900714.RAJA21B61A3DmqbR4owD5_coFtRF64c8RiLyDEFw0rrDI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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" .
}