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- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion type Assertion NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_head.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion wasGeneratedBy ECO_0000218 NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion wasDerivedFrom uniprot-2016 NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion SIO_000772 8136837 NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion evidence source_evidence_curated NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.
- NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_assertion description "[Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8765.RAD9Dq8cN1406Boe7Pbyy724vEPV8FaHbfwiwJGenhKaU130_provenance.