Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_assertion> ?p ?o ?g. }
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- NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_assertion type Assertion NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_head.
- NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_assertion wasGeneratedBy ECO_0000203 NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_provenance.
- NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_assertion wasDerivedFrom befree-2016 NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_provenance.
- NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_assertion SIO_000772 21616938 NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_provenance.
- NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_assertion evidence source_evidence_literature NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_provenance.
- NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_assertion description "[A homozygous mutation in the RAD51C gene was recently found to cause Fanconi anemia-like disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897092.RADeiQtucoQS9q-BpSYMaVtTHfbxRa7AKI2VOpYpQIOhE130_provenance.