Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_assertion description "[Mutations in SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_assertion evidence source_evidence_literature NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_assertion SIO_000772 17273969 NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_assertion wasDerivedFrom lhgdn-20090331 NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_assertion wasGeneratedBy ECO_0000203 NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.