Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.
- NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_assertion wasGeneratedBy ECO_0000203 NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.
- NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_assertion wasDerivedFrom befree-20150227 NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.
- NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_assertion SIO_000772 10737122 NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.
- NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_assertion evidence source_evidence_literature NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.
- NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_assertion 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." NP322782.RAXIgpmpYXWPWPHb2Yn2xovT9SfMUzWpnuT8h4r2IL2L4130_provenance.