Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_assertion> ?p ?o ?g. }
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- NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_assertion type Assertion NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_head.
- NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_assertion description "[Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.
- NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_assertion evidence source_evidence_literature NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.
- NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_assertion SIO_000772 21882291 NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.
- NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_assertion wasDerivedFrom befree-20150227 NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.
- NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_assertion wasGeneratedBy ECO_0000203 NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.