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- NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_assertion type Assertion NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_head.
- NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_assertion wasGeneratedBy ECO_0000203 NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_provenance.
- NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_assertion wasDerivedFrom befree-20150227 NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_provenance.
- NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_assertion SIO_000772 23714752 NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_provenance.
- NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_assertion evidence source_evidence_literature NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_provenance.
- NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_assertion description "[Whereas mutations in COL4A5 and contiguous X-chromosomal deletions involving COL4A5 and COL4A6 are associated with X-linked Alport syndrome, a nephropathy associated with deafness and cataract, mutations in COL4A6 alone have not been related to any hereditary disease so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320192.RAJVaTP8jFsLn_oEf5TncH5xVDsjQG62_-1j83EfY1z1w130_provenance.