Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.
- NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_assertion description "[Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.
- NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_assertion evidence source_evidence_literature NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.
- NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_assertion SIO_000772 15805154 NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.
- NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_assertion wasDerivedFrom befree-20140225 NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.
- NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_assertion wasGeneratedBy ECO_0000203 NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP806492.RAUK_2muzPQMGCICHQQ1i3Cu0PqTV4MU4SbBGUsx6uQbk130_provenance.