Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_assertion> ?p ?o ?g. }
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- NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_assertion type Assertion NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_head.
- NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_assertion wasGeneratedBy ECO_0000203 NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_provenance.
- NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_assertion wasDerivedFrom befree-20140225 NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_provenance.
- NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_assertion SIO_000772 23318428 NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_provenance.
- NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_assertion evidence source_evidence_literature NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_provenance.
- NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_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." NP863159.RA9bQH8kllKdxEn_pPIV0NeZVd2hf3YGHW6ncewVOXg3U130_provenance.