Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.
- 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.
- uniprot-20130724 importedOn "2013-07-24" NP3121.RAa5vttqols3oiBH6xosNZIWloAgiFqDQBpFOH9j-PhyY130_provenance.