Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_assertion> ?p ?o ?g. }
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- NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_assertion type Assertion NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_head.
- NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_assertion description "[The mutation frequencies among distinct phenotypes were 85% for BSS, 100% for FC, and 44% for MFT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_provenance.
- NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_assertion evidence source_evidence_curated NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_provenance.
- NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_assertion SIO_000772 18234730 NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_provenance.
- NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_assertion wasDerivedFrom ctd_human-20150221 NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_provenance.
- NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_assertion wasGeneratedBy ECO_0000218 NP11980.RAQDrCl4S4oAvZpeoUIO5CSpokk1hN7OW9MsxGvPz88yI130_provenance.