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- source_evidence_literature type ECO_0000212 NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.
- NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_assertion wasGeneratedBy ECO_0000203 NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.
- NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_assertion wasDerivedFrom befree-20140225 NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.
- NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_assertion SIO_000772 11576738 NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.
- NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_assertion evidence source_evidence_literature NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.
- NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_assertion description "[Myotonic dystrophy (DM), Huntington's disease (HD) and Fragile X syndrome (FRAXA) are three monogenic disease which are caused by so-called dynamic mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP857069.RAEUv3DG-7m7khBqW1hIGh3e7zSnRjNyUCp4_569UfEHk130_provenance.