Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.
- NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_assertion wasGeneratedBy ECO_0000203 NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.
- NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_assertion wasDerivedFrom befree-20140225 NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.
- NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_assertion SIO_000772 7508181 NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.
- NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_assertion evidence source_evidence_literature NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.
- NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_assertion description "[Recent studies in our laboratory established genetic linkage to the type II keratin gene locus on chromosome 12q in one family with EH and identified a single amino acid mutation in keratin 1 that is responsible for the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP595328.RAvRXQMo4ysMQ0hLV44SY1ODS9AK9_MuL4Y0-2Mc7Fyyk130_provenance.