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- NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_assertion type Assertion NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_head.
- NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_assertion wasGeneratedBy ECO_0000203 NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_provenance.
- NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_assertion wasDerivedFrom befree-2016 NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_provenance.
- NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_assertion SIO_000772 22512561 NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_provenance.
- NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_assertion evidence source_evidence_literature NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_provenance.
- NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_provenance.