Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_assertion type Assertion NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_head.
- NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_assertion wasGeneratedBy ECO_0000203 NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_provenance.
- NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_assertion wasDerivedFrom befree-20150227 NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_provenance.
- NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_assertion SIO_000772 20949621 NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_provenance.
- NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_assertion evidence source_evidence_literature NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_provenance.
- NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_assertion description "[Germline KRAS mutations were shown recently to be associated with developmental disorders, including Noonan syndrome (NS), cardio-facio-cutaneous syndrome (CFCS), and Costello syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527416.RAJze-O1dKoirT5VHGI1PoJ4Zzg3UD7phoZoELO4bHsh4130_provenance.