Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.
- NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_assertion description "[Hypophosphatasia is a rare inherited disorder characterized by defective bone mineralization and deficiency of serum and liver/bone/kidney-type alkaline phosphatase (L/B/K ALP) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.
- NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_assertion evidence source_evidence_literature NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.
- NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_assertion SIO_000772 10679946 NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.
- NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_assertion wasDerivedFrom befree-20150227 NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.
- NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_assertion wasGeneratedBy ECO_0000203 NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP947979.RAUuqy7t-2zD53Fnnf6_voyRe0tcvfj7ubrjnlwLW8QKM130_provenance.