Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_assertion> ?p ?o ?g. }
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- NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_assertion type Assertion NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_head.
- NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_assertion wasGeneratedBy ECO_0000218 NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.
- NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_assertion wasDerivedFrom uniprot-20130724 NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.
- NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_assertion SIO_000772 17054105 NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.
- NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_assertion evidence source_evidence_curated NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.
- NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_assertion description "[Diversity, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.