Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_assertion> ?p ?o ?g. }
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- NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_assertion type Assertion NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_head.
- NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_assertion wasGeneratedBy ECO_0000203 NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_provenance.
- NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_assertion wasDerivedFrom befree-2016 NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_provenance.
- NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_assertion SIO_000772 24935154 NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_provenance.
- NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_assertion evidence source_evidence_literature NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_provenance.
- NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_provenance.