Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_assertion type Assertion NP601764.RAgf80G3G8pEY0KpMMkjtP0yF0zLees0xJvLs1Z_Lqf5w130_head.
- 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.