Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_assertion type Assertion NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_head.
- NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_assertion description "[Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_provenance.
- NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_assertion evidence source_evidence_literature NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_provenance.
- NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_assertion SIO_000772 7657792 NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_provenance.
- NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_assertion wasDerivedFrom befree-2016 NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_provenance.
- NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_assertion wasGeneratedBy ECO_0000203 NP1316809.RA33Wm_QlDeHivY5dhFobxTST6LERkL78OCwij2nSW694130_provenance.