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- source_evidence_literature type ECO_0000212 NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.
- NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_assertion description "[In this study, NR2E3 mutations (p.G56R, p.V118M) were found to be responsible for approximately 2.9% of overall RP in Chinese patients, comparable to the contributions of RHO and RP1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.
- NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_assertion evidence source_evidence_literature NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.
- NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_assertion SIO_000772 19933183 NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.
- NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_assertion wasDerivedFrom befree-20150227 NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.
- NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_assertion wasGeneratedBy ECO_0000203 NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP834407.RA0V70IHFZ6UMmeT6NJc4f_k0tfexeTyJ3nGp076XQNZ4130_provenance.