Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_assertion> ?p ?o ?g. }
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- NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_assertion type Assertion NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_head.
- NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_assertion description "[Missense mutations in the BCS1L gene as a cause of the Bj�rnstad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_provenance.
- NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_assertion evidence source_evidence_curated NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_provenance.
- NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_assertion SIO_000772 17314340 NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_provenance.
- NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_assertion wasDerivedFrom uniprot-2016 NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_provenance.
- NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_assertion wasGeneratedBy ECO_0000218 NP4879.RAPpHG-L_Fu-7vW8Sn8XcK3OzJXglI9ECb3VrTAKiJb9c130_provenance.