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- source_evidence_literature type ECO_0000212 NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_assertion description "[We performed mutational analysis of MNX1 in all cases by DNA sequencing as well as by Multiplex Ligation-dependent Probe Amplification (MLPA) in those CS cases where no MNX1 mutations were found, to exclude a MNX1 heterozygous loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_assertion evidence source_evidence_literature NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_assertion SIO_000772 24095820 NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_assertion wasDerivedFrom befree-20150227 NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_assertion wasGeneratedBy ECO_0000203 NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP452506.RARnjCuE-s2lvIq6hXbE0x_dE2YHSr7kfsnOgQWO5ZQGQ130_provenance.