Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_assertion> ?p ?o ?g. }
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- NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_assertion type Assertion NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_head.
- NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_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." NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_provenance.
- NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_assertion evidence source_evidence_literature NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_provenance.
- NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_assertion SIO_000772 11317367 NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_provenance.
- NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_assertion wasDerivedFrom befree-2016 NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_provenance.
- NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_assertion wasGeneratedBy ECO_0000203 NP315711.RAhe6bFggxLp3iohdPz2mvhAVT8wVp3rRr48dlD6Ra6WE130_provenance.