Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.
- NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_assertion description "[A novel STX16 deletion in autosomal dominant pseudohypoparathyroidism type Ib redefines the boundaries of a cis-acting imprinting control element of GNAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.
- NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_assertion evidence source_evidence_literature NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.
- NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_assertion SIO_000772 15800843 NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.
- NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_assertion wasDerivedFrom befree-20150227 NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.
- NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_assertion wasGeneratedBy ECO_0000203 NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP801771.RARsA5gpA0jQec7t4U6SfMVd6xp5dcj8pPGRNWqcQ8yFM130_provenance.