Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_assertion> ?p ?o ?g. }
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- NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_assertion type Assertion NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_head.
- NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_assertion description "[Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_provenance.
- NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_assertion evidence source_evidence_literature NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_provenance.
- NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_assertion SIO_000772 15146470 NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_provenance.
- NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_assertion wasDerivedFrom befree-2016 NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_provenance.
- NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_assertion wasGeneratedBy ECO_0000203 NP444352.RAuGrZ8rDtFp0vDhiDjwEm7rRgSR0UfpUjuqm6N1i8pI8130_provenance.