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- source_evidence_literature type ECO_0000212 NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion evidence source_evidence_literature NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion SIO_000772 18499664 NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion wasDerivedFrom befree-20150227 NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion wasGeneratedBy ECO_0000203 NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.