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- source_evidence_literature type ECO_0000212 NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.
- NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_assertion description "[Mutations in the human RDS gene are responsible for several forms of inherited blindness including autosomal-dominant retinitis pigmentosa and macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.
- NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_assertion evidence source_evidence_literature NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.
- NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_assertion SIO_000772 10704489 NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.
- NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_assertion wasDerivedFrom befree-20150227 NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.
- NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_assertion wasGeneratedBy ECO_0000203 NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP760975.RAS3VE6Eypo96A_BkGN37hiNurxEgmW_-oMI8_HrIznlo130_provenance.