Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.
- NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_assertion description "[We studied a large Swiss family with dominantly inherited hereditary spherocytosis and band 3 (anion exchanger 1, AE1) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.
- NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_assertion evidence source_evidence_literature NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.
- NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_assertion SIO_000772 8547122 NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.
- NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_assertion wasDerivedFrom befree-20140225 NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.
- NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_assertion wasGeneratedBy ECO_0000203 NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP665491.RAKcNXiJYQNdWJ5QSkicXrOw9950KXbD0426ZkfQ3MaZA130_provenance.