Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion> ?p ?o ?g. }
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- NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion type Assertion NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_head.
- NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_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." NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_provenance.
- NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion evidence source_evidence_literature NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_provenance.
- NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion SIO_000772 11317367 NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_provenance.
- NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion wasDerivedFrom befree-2016 NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_provenance.
- NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_assertion wasGeneratedBy ECO_0000203 NP315712.RAGBLm7VY6T9ug4SIcCIsTa4PccNe60u_Aby2vXcqrivY130_provenance.