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- NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_assertion type Assertion NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_head.
- NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_assertion wasGeneratedBy ECO_0000203 NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_provenance.
- NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_assertion wasDerivedFrom befree-2016 NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_provenance.
- NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_assertion SIO_000772 17177198 NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_provenance.
- NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_assertion evidence source_evidence_literature NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_provenance.
- NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_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." NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_provenance.