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- source_evidence_literature type ECO_0000212 NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.
- NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_assertion description "[Coexistence of KCNV2 associated cone dystrophy with supernormal rod electroretinogram and MFRP related oculopathy in a Turkish family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.
- NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_assertion evidence source_evidence_literature NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.
- NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_assertion SIO_000772 23143909 NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.
- NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_assertion wasDerivedFrom befree-20150227 NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.
- NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_assertion wasGeneratedBy ECO_0000203 NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978026.RA5Olcwkn0I5U-FS1w1aolBx0l4k6BAYVrNm1hfeB5QjU130_provenance.