Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.
- NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_assertion description "[MHA and SBS can be differentiated by subtle ultrastructural leukocyte inclusion features, whereas FTNS is distinguished by the additional Alport-like clinical features of sensorineural deafness, cataracts and nephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.
- NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_assertion evidence source_evidence_literature NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.
- NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_assertion SIO_000772 10973259 NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.
- NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_assertion wasDerivedFrom befree-20140225 NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.
- NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_assertion wasGeneratedBy ECO_0000203 NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP618959.RAgHdNMlOUNoPV_XkObEYb31jjHMIA70LkCrWcJ11jbxk130_provenance.