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- source_evidence_literature type ECO_0000212 NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.
- NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_assertion description "[Mutation screening and DNA sequencing of the MET gene, which is mapped to 7q31, revealed only the presence of simple sequence polymorphisms but no apparent acquired disease-associated mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.
- NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_assertion evidence source_evidence_literature NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.
- NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_assertion SIO_000772 9485032 NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.
- NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_assertion wasDerivedFrom befree-20150227 NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.
- NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_assertion wasGeneratedBy ECO_0000203 NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP803026.RABK8TGoRHSogk0dC3S5GyS5JjNjJmS26JhW6AQUB09xg130_provenance.