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- NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_assertion type Assertion NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_head.
- NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_assertion wasGeneratedBy ECO_0000203 NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_provenance.
- NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_assertion wasDerivedFrom befree-20140225 NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_provenance.
- NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_assertion SIO_000772 17054105 NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_provenance.
- NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_assertion evidence source_evidence_literature NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_provenance.
- NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_assertion description "[To further investigate the phenotypic spectrum associated with germline HRAS mutations and characterize their molecular diversity, subjects with a diagnosis of CS (N = 9), Noonan syndrome (NS; N = 36), cardiofaciocutaneous syndrome (CFCS; N = 4), or with a phenotype suggestive of these conditions but without a definitive diagnosis (N = 12) were screened for the entire coding sequence of the gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808579.RAA4Tf4wIx2qh91l8X7PqSWbYLgimv2_sp139pSr-uL8o130_provenance.