Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_assertion> ?p ?o ?g. }
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- NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_assertion type Assertion NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_head.
- NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_assertion wasGeneratedBy ECO_0000218 NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_provenance.
- NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_assertion wasDerivedFrom uniprot-20130724 NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_provenance.
- NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_assertion SIO_000772 16642020 NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_provenance.
- NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_assertion evidence source_evidence_curated NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_provenance.
- NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_assertion description "[Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4279.RARM9nLd4LuGeqtP5TA1_Ym6RPUtiLzYbv196VhF5VikA130_provenance.