Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.
- NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_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." NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.
- NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_assertion evidence source_evidence_literature NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.
- NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_assertion SIO_000772 20125191 NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.
- NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_assertion wasDerivedFrom befree-2016 NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.
- NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_assertion wasGeneratedBy ECO_0000203 NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.
- befree-2016 importedOn "2016-02-19" NP791223.RA5omJx7YZGm-1ocrNbdWQj_UVZ7Vk74YwWeWOUP5HEKk130_provenance.