Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_assertion> ?p ?o ?g. }
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- NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_assertion type Assertion NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_head.
- NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_assertion wasGeneratedBy ECO_0000218 NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_provenance.
- NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_assertion wasDerivedFrom uniprot-2016 NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_provenance.
- NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_assertion SIO_000772 10528858 NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_provenance.
- NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_assertion evidence source_evidence_curated NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_provenance.
- NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_assertion description "[Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429.RAD4-bfMuBTQIhXO8ZgyH1d2z4B0GHGa-v1thKQaeFxrE130_provenance.