Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_assertion type Assertion NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_head.
- NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_assertion wasGeneratedBy ECO_0000203 NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.
- NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_assertion wasDerivedFrom befree-20140225 NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.
- NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_assertion SIO_000772 16908353 NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.
- NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_assertion evidence source_evidence_literature NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.
- NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_assertion description "[While a chromosome 14 inversion is highly characteristic, additional inherent cytogenetic differences, such as trisomy 8 with CMYC over-amplification, may account for some case to case variation in clinical course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.