Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_assertion> ?p ?o ?g. }
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- NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_assertion type Assertion NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_head.
- NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_assertion wasGeneratedBy ECO_0000203 NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_provenance.
- NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_assertion wasDerivedFrom befree-2016 NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_provenance.
- NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_assertion SIO_000772 23318428 NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_provenance.
- NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_assertion evidence source_evidence_literature NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_provenance.
- NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_assertion description "[Overexpression of either Shp2Thr468Met (a phosphatase-defective mutant found in Lentigines, Electrocardiographic abnormalities, Ocular hypertelorism, Pulmonary stenosis, Abnormal genitalia, Retardation of growth and sensorineural Deafness (LEOPARD) syndrome) or Shp2Asn308Asp (a phosphatase-active mutant found in Noonan syndrome) with EphA2 exhibited comparable activation of Erk and stronger activation than wild-type Shp2, suggesting the phosphatase-independent Erk activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1043676.RAO9iAJmYp1OTlFHw37rWz0EFvX2Or88SRzn37NWhWAtc130_provenance.