Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_assertion> ?p ?o ?g. }
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- NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_assertion type Assertion NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_head.
- NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_assertion description "[The Duchenne/Becker muscular dystrophy (DMD/BMD) is caused by mutations in the dystrophin gene, which is located on chromosome Xp21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_provenance.
- NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_assertion evidence source_evidence_literature NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_provenance.
- NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_assertion SIO_000772 19009915 NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_provenance.
- NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_assertion wasDerivedFrom befree-2016 NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_provenance.
- NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_assertion wasGeneratedBy ECO_0000203 NP703390.RAdzsiAD2y52WStk-MA_D2c_Hk16BXgfPthasc4I7yqfM130_provenance.