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- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion type Assertion NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_head.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion description "[Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion evidence source_evidence_literature NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion SIO_000772 21340158 NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion wasDerivedFrom befree-2016 NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.
- NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_assertion wasGeneratedBy ECO_0000203 NP874166.RAMOSKd96c_XP6W-0XjLKnzT9Za0SHCaif9E5r920Rs7c130_provenance.