Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_assertion> ?p ?o ?g. }
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- NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_assertion type Assertion NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_head.
- NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_assertion wasGeneratedBy ECO_0000203 NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_provenance.
- NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_assertion wasDerivedFrom befree-2016 NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_provenance.
- NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_assertion SIO_000772 11257260 NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_provenance.
- NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_assertion evidence source_evidence_literature NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_provenance.
- NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311450.RAxM-oM26Z35Xkj3frHFAQIx4MvIhm71BI4-cOPZiNlvo130_provenance.