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- NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_assertion type Assertion NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_head.
- 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.