Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_assertion> ?p ?o ?g. }
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- NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_assertion type Assertion NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_head.
- NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_assertion wasGeneratedBy ECO_0000203 NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_provenance.
- NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_assertion wasDerivedFrom befree-20140225 NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_provenance.
- NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_assertion SIO_000772 20030748 NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_provenance.
- NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_assertion evidence source_evidence_literature NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_provenance.
- NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_assertion description "[Germline mutations in several members of RAS/RAF/MEK/ERK pathway cause clinically similar genetic disorders, including Noonan syndrome (NS), Costello syndrome (CS) and cardio-facio-cutaneous syndrome (CFC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411421.RAAP08avhMypQqDrGPTih-bRuQAvZFJZlnuH6OJxyB41w130_provenance.