Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.
- NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_assertion description "[The map encompasses all the candidate loci of Bardet-Biedle syndrome type I (BBS1) and spinocerebellar ataxia type 5 (SCA5), one-third of the distal region for hereditary paraganglioma 2 (PGL2), and one-third of the central region for insulin-dependent diabetes mellitus 4 (IDDM4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.
- NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_assertion evidence source_evidence_literature NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.
- NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_assertion SIO_000772 9405936 NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.
- NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_assertion wasDerivedFrom befree-20140225 NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.
- NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_assertion wasGeneratedBy ECO_0000203 NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401669.RAJNBV7cd1SxJWplc_tzcOT7Mss-H_N89EWz0reF49vDM130_provenance.