Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP932622.RAfB3AySdxu7BeV8FzaBWKAmdTGAB9GoS1CaNLHMQN5H4130_provenance.