Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.
- NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_assertion description "[Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.
- NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_assertion evidence source_evidence_literature NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.
- NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_assertion SIO_000772 11443188 NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.
- NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_assertion wasDerivedFrom befree-2016 NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.
- NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_assertion wasGeneratedBy ECO_0000203 NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.
- befree-2016 importedOn "2016-02-19" NP323128.RAKf5bZ5KJrUf-xpoI0yNAjRlJvwJvvr0uy4pozZUrk1g130_provenance.