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- source_evidence_literature type ECO_0000212 NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.
- NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_assertion description "[We conclude that molecular diagnosis is a necessary adjunct for clinical diagnosis and management of inherited and sporadic neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.
- NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_assertion evidence source_evidence_literature NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.
- NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_assertion SIO_000772 11835375 NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.
- NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_assertion wasDerivedFrom gad-20150221 NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.
- NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_assertion wasGeneratedBy ECO_0000203 NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP72850.RAIVpe-d6iaSEMbrF6WqzljLxXfZl7-PbAGhgBrexoPvA130_provenance.