Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.
- NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_assertion description "[Direct sequencing analysis showed that all mutations were CAA (Gln) to CGA (Arg) transition of codon 61, except for CAA to AAA transversion in one case of follicular carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.
- NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_assertion evidence source_evidence_literature NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.
- NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_assertion SIO_000772 7704243 NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.
- NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_assertion wasDerivedFrom befree-2016 NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.
- NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_assertion wasGeneratedBy ECO_0000203 NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1319005.RAjHeUDv4ykj2tLR2xFfXE9yIydbP5QtyLglnIb1iVzkM130_provenance.