Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.
- NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_assertion description "[DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.
- NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_assertion evidence source_evidence_literature NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.
- NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_assertion SIO_000772 23109149 NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.
- NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_assertion wasDerivedFrom befree-20150227 NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.
- NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_assertion wasGeneratedBy ECO_0000203 NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP806389.RARdE77KAg_gS6fUv-TgfVgvEGX8ZK0JqBqaMg23IL7t8130_provenance.