Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.
- NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_assertion description "[A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.
- NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_assertion evidence source_evidence_literature NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.
- NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_assertion SIO_000772 9837820 NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.
- NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_assertion wasDerivedFrom befree-2016 NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.
- NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_assertion wasGeneratedBy ECO_0000203 NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1410101.RAFFEjBwmc9DosWyDnhT6nN5IUi2bG4T54ES_aoIcuNQQ130_provenance.