Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_assertion> ?p ?o ?g. }
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- NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_assertion type Assertion NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_head.
- NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_assertion description "[Mutation in FANCI is responsible for loss of a functional FA pathway in a patient with Fanconi anemia complementation group I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_provenance.
- NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_assertion evidence source_evidence_literature NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_provenance.
- NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_assertion SIO_000772 17412408 NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_provenance.
- NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_assertion wasDerivedFrom befree-20140225 NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_provenance.
- NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_assertion wasGeneratedBy ECO_0000203 NP516897.RAalCPPRwamb5wZk7jQ2rua48lYQlkh6UKfEUXhbHYQpg130_provenance.