Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_assertion> ?p ?o ?g. }
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- NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_assertion type Assertion NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_head.
- NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_assertion wasGeneratedBy ECO_0000203 NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_provenance.
- NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_assertion wasDerivedFrom befree-20140225 NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_provenance.
- NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_assertion SIO_000772 20030748 NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_provenance.
- NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_assertion evidence source_evidence_literature NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_provenance.
- NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_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." NP901958.RA88gBCaM5ITxuooqMazA2xA5Y3SE4Z7E64wc6mDSDQwc130_provenance.