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- source_evidence_literature type ECO_0000212 NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.
- NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_assertion description "[The other mutation detected in MLH1 was a TAC-->TAA substitution codon 750 (exon 19) creating a stop codon, predicted to generate a truncated protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.
- NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_assertion evidence source_evidence_literature NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.
- NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_assertion SIO_000772 11369138 NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.
- NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_assertion wasDerivedFrom befree-2016 NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.
- NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_assertion wasGeneratedBy ECO_0000203 NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.
- befree-2016 importedOn "2016-02-19" NP318632.RAFMHajT0w45_CZH8xf375FFOjsK3z0UNn82TOWL01GXM130_provenance.