Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.
- NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_assertion description "[Fabry disease is an X-linked lysosomal storage disorder due to deficient activity of alpha-galactosidase A (?-Gal A) leading to renal insufficiency in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.
- NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_assertion evidence source_evidence_literature NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.
- NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_assertion SIO_000772 23190516 NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.
- NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_assertion wasDerivedFrom befree-20140225 NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.
- NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_assertion wasGeneratedBy ECO_0000203 NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP460957.RAfTgzzJU7dOX7Itls35Vqs3QYhXpVyq03oc9xyLO8UDM130_provenance.