Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_assertion> ?p ?o ?g. }
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- NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_assertion type Assertion NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_head.
- NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_assertion wasGeneratedBy ECO_0000203 NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.
- NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_assertion wasDerivedFrom befree-20150227 NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.
- NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_assertion SIO_000772 23446638 NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.
- NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_assertion evidence source_evidence_literature NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.
- NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_assertion description "[KLLN variants in CS/CSL patients are rare (1 of 136, 0.007%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.