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- source_evidence_literature type ECO_0000212 NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.
- NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_assertion description "[To detect chromosomal rearrangements indicating novel positional candidate RSTS genes, we used a-CGH to study 26 patients fulfilling the diagnostic criteria for RSTS who were negative at fluorescence in situ hybridisation analyses of the CREBBP and EP300 regions, and direct sequencing analyses of the CREBBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.
- NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_assertion evidence source_evidence_literature NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.
- NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_assertion SIO_000772 20125191 NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.
- NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_assertion wasDerivedFrom befree-2016 NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.
- NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_assertion wasGeneratedBy ECO_0000203 NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.
- befree-2016 importedOn "2016-02-19" NP791224.RA44m7h-U-uXJlkz5QLF4LftUtLzdoCWNI7nZqhMrs-fE130_provenance.