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- source_evidence_literature type ECO_0000212 NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.
- NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.
- NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_assertion evidence source_evidence_literature NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.
- NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_assertion SIO_000772 22158539 NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.
- NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_assertion wasDerivedFrom befree-2016 NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.
- NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_assertion wasGeneratedBy ECO_0000203 NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.
- befree-2016 importedOn "2016-02-19" NP945704.RANwsZcpE00g4dck2gsNG8PilZiuNtYnXl92-LNPfz8l0130_provenance.