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- NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_assertion type Assertion NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_head.
- NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_assertion description "[Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_provenance.
- NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_assertion evidence source_evidence_literature NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_provenance.
- NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_assertion SIO_000772 23304067 NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_provenance.
- NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_assertion wasDerivedFrom befree-2016 NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_provenance.
- NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_assertion wasGeneratedBy ECO_0000203 NP1042464.RAiWb9YHWlT5VnR_Fmz43JDDF1-g8HL8lT8P4Yn5jNGjg130_provenance.