Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.
- NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_assertion description "[GCAP1 mutations associated with autosomal dominant cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.
- NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_assertion evidence source_evidence_literature NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.
- NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_assertion SIO_000772 20238026 NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.
- NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_assertion wasDerivedFrom befree-20140225 NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.
- NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_assertion wasGeneratedBy ECO_0000203 NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP924792.RAlpFGzH4sKQVQ8hD8VahTOSXC8_V7opwnzkh0VcEDulg130_provenance.