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- source_evidence_literature type ECO_0000212 NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.
- NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_assertion wasGeneratedBy ECO_0000203 NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.
- NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_assertion wasDerivedFrom befree-2016 NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.
- NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_assertion SIO_000772 17177198 NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.
- NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_assertion evidence source_evidence_literature NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.
- NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.