Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_assertion> ?p ?o ?g. }
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- NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_assertion type Assertion NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_head.
- NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_assertion wasGeneratedBy ECO_0000218 NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_provenance.
- NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_assertion wasDerivedFrom uniprot-2016 NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_provenance.
- NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_assertion SIO_000772 17054105 NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_provenance.
- NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_assertion evidence source_evidence_curated NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_provenance.
- NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_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." NP4739.RADlNjdNGOc9MJw0tfNoA7Ma4PoLi8JF0teZXQNJFO5Ls130_provenance.