Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.
- NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_assertion description "[Clinical phenotypes include CMT1B, CMT2, Dejerine-Sottas syndrome, and congenital hypomyelination neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.
- NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_assertion evidence source_evidence_literature NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.
- NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_assertion SIO_000772 22622165 NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.
- NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_assertion wasDerivedFrom befree-20140225 NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.
- NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_assertion wasGeneratedBy ECO_0000203 NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP673212.RABEgQpehNyETOY8hj_chM7EgDiKhyKcbW7ZWQeJaTyTg130_provenance.