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- source_evidence_literature type ECO_0000212 NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion evidence source_evidence_literature NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion SIO_000772 12676894 NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion wasDerivedFrom befree-2016 NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion wasGeneratedBy ECO_0000203 NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- befree-2016 importedOn "2016-02-19" NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.