Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_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." NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_assertion evidence source_evidence_literature NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_assertion SIO_000772 17273969 NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_assertion wasDerivedFrom lhgdn-20090331 NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_assertion wasGeneratedBy ECO_0000203 NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.