Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.
- NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_assertion description "[In this study, four new K12 mutations (Arg135Gly, Arg135Ile, Tyr429Asp, and Leu140Arg) were identified in three unrelated MCD pedigrees and in one individual with MCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.
- NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_assertion evidence source_evidence_literature NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.
- NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_assertion SIO_000772 9399908 NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.
- NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_assertion wasDerivedFrom befree-2016 NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.
- NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_assertion wasGeneratedBy ECO_0000203 NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.
- befree-2016 importedOn "2016-02-19" NP1385439.RAdfONLKKgVJCA3_WfrkC-ZNygBu0O_nrJTEsbE-ShTro130_provenance.