Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_assertion> ?p ?o ?g. }
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- NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_assertion type Assertion NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_head.
- NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_assertion wasGeneratedBy ECO_0000203 NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_provenance.
- NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_assertion wasDerivedFrom befree-20140225 NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_provenance.
- NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_assertion SIO_000772 8530067 NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_provenance.
- NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_assertion evidence source_evidence_literature NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_provenance.
- NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_assertion description "[Two forms of inherited childhood nonsyndromic deafness (DFNB1 and DFNA3) and a Duchenne-like form of progressive muscular dystrophy (LGMD2C) have been mapped to the pericentromeric region of chromosome 13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359746.RAy9lj0GO30l78OTraRma2-HHoYaN_hwxullRsEzDeH5U130_provenance.