Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_assertion> ?p ?o ?g. }
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- NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_assertion type Assertion NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_head.
- NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_assertion description "[In an African American population in which autosomal recessive Alport syndrome is rarely seen, complete sequencing of the COL4A3 and COL4A4 genes may be necessary to identify the underlying mutation and confirm the diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_provenance.
- NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_assertion evidence source_evidence_literature NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_provenance.
- NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_assertion SIO_000772 18436078 NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_provenance.
- NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_assertion wasDerivedFrom befree-20140225 NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_provenance.
- NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_assertion wasGeneratedBy ECO_0000203 NP608837.RAeg3Y-huRYSOYnT4qowhZnAk-avml1WqQ--z5SPEuYjc130_provenance.