Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_assertion> ?p ?o ?g. }
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- NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_assertion type Assertion NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_head.
- NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_assertion description "[Heterozygous truncating mutations in the RP1 gene cause approximately 7% of autosomal dominant retinitis pigmentosa (RP) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_provenance.
- NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_assertion evidence source_evidence_literature NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_provenance.
- NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_assertion SIO_000772 11317367 NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_provenance.
- NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_assertion wasDerivedFrom befree-20140225 NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_provenance.
- NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_assertion wasGeneratedBy ECO_0000203 NP404168.RABea_basnyL5IX_tljk4OX2rkQm4tRqMazW1XUku6_Fo130_provenance.