Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1013031.RAyhLabboaV1m1U7Z8oNnwae9h8UQOGZ8RhCCYDgDMr_8130_provenance.
- 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.