Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_assertion type Assertion NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_head.
- NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_assertion description "[To examine the role of RP1 mutations in RP, we screened 101 unrelated Chinese RP patients (unselected for mode of inheritance) and 190 elderly normal control subjects for sequence changes in the coding exons for the 2156 amino acid RP1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_provenance.
- NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_assertion evidence source_evidence_literature NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_provenance.
- NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_assertion SIO_000772 11317367 NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_provenance.
- NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_assertion wasDerivedFrom befree-2016 NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_provenance.
- NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_assertion wasGeneratedBy ECO_0000203 NP315713.RAGRyoQGeE6yrIsid2XanbbskpKBUk0Ss8LpsEMOmwtPk130_provenance.