Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_assertion wasGeneratedBy ECO_0000203 NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_assertion wasDerivedFrom befree-20150227 NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_assertion SIO_000772 23273231 NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_assertion evidence source_evidence_literature NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.
- NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_assertion description "[α-1 antitrypsin (AAT) deficiency is one of the most important genetic causes of childhood liver diseases in some parts of the world, but its geographic distribution is highly variable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619849.RACd1UdKOcMcdaUSH9r-U0Dzz-Z1O8eL4jWCHVIkf0_Wc130_provenance.