Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_assertion type Assertion NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_head.
- 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.