Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_assertion> ?p ?o ?g. }
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- NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_assertion type Assertion NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_head.
- NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_provenance.
- NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_assertion evidence source_evidence_literature NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_provenance.
- NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_assertion SIO_000772 8595413 NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_provenance.
- NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_assertion wasDerivedFrom befree-20140225 NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_provenance.
- NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_assertion wasGeneratedBy ECO_0000203 NP625789.RAV4e2hdBBOlTQdVnG_wzeBNA7Gta2AmcGSx-Pq5p77eY130_provenance.