Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_assertion> ?p ?o ?g. }
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- NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_assertion type Assertion NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_head.
- NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_assertion description "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_provenance.
- NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_assertion evidence source_evidence_curated NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_provenance.
- NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_assertion SIO_000772 23453666 NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_provenance.
- NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_assertion wasDerivedFrom uniprot-2016 NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_provenance.
- NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_assertion wasGeneratedBy ECO_0000218 NP7380.RAOSgLuwpeNyp7YOnC81MwdN2M4DnEVuUNaK3b4KXPCLw130_provenance.