Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_assertion> ?p ?o ?g. }
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- NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_assertion type Assertion NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_head.
- NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_assertion description "[Although medulloblastoma is a component of Turcot syndrome with demonstrated APC mutations, APC gene deletions appear to be absent or very uncommon in patients with sporadic and NBCCS-associated medulloblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_provenance.
- NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_assertion evidence source_evidence_literature NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_provenance.
- NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_assertion SIO_000772 10375116 NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_provenance.
- NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_assertion wasDerivedFrom befree-20150227 NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_provenance.
- NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_assertion wasGeneratedBy ECO_0000203 NP647882.RAVu_2zUaTqCakVpXZyP1umEwMi7thjcJiFxx1UlKGzIQ130_provenance.