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- source_evidence_literature type ECO_0000212 NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP978023.RAtI_N7b4X3yNX_Kn97kN2NHP4C3le64Cqu5ppOlas3do130_provenance.