@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_head { this: np:hasAssertion dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_assertion; np:hasProvenance dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_provenance; np:hasPublicationInfo dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_publicationInfo; a np:Nanopublication . dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_assertion a np:Assertion . dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_provenance a np:Provenance . dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_publicationInfo a np:PublicationInfo . } dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_assertion { miriam-gene:119 a ncit:C16612 . lld:C1850808 a ncit:C7057 . dgn-gda:DGN57425e7af7f3d0540cc49ef75091a8eb sio:SIO_000628 miriam-gene:119, lld:C1850808; a sio:SIO_001121 . } dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_provenance { dgn-np:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_assertion dcterms:description "[In this study we have: (1) detected recombination events with the disease locus in one family, placing the MM gene most likely between markers D2S443 (CHLC.GGAA4D07.1876) and D2S2109; (2) generated a yeast artificial chromosome contig that spans approximately 3.8 megabases and extends from marker D2S358 to marker D2S286; (3) physically mapped 21 polymorphic markers, 5 genes, 3 STSs, and 1 EST within this contig; (4) detected and mapped a new polymorphism within this interval, allowing us to further reduce the MM locus to a 360-kilobase segment; (5) mapped the gene for the cytoskeletal protein beta-adducin within the MM candidate region, failing to find a consistent pattern of mutation of this gene in our MM patients; (6) excluded seven other candidate myopathy genes from the Miyoshi locus.]. 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:10737122; 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:NP442448.RABeX47-fPPwkxyfO2Ddf3DAbl7J8ZAZAbcEkuzUGPo84130_publicationInfo { this: dcterms:created "2014-10-02T12:36:24+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }