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- source_evidence_literature type ECO_0000212 NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.
- NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_assertion description "[Using the Universal Mutation Database (UMD) software, we have constructed `UMD-USHbases`, a set of relational databases of nucleotide variations for seven genes involved in Usher syndrome (MYO7A, CDH23, PCDH15, USH1C, USH1G, USH3A and USH2A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.
- NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_assertion evidence source_evidence_literature NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.
- NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_assertion SIO_000772 18484607 NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.
- NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_assertion wasDerivedFrom befree-20140225 NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.
- NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_assertion wasGeneratedBy ECO_0000203 NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_provenance.