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- NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_assertion type Assertion NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_head.
- NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_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." NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_provenance.
- NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_assertion evidence source_evidence_literature NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_provenance.
- NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_assertion SIO_000772 17273969 NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_provenance.
- NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_assertion wasDerivedFrom lhgdn-20090331 NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_provenance.
- NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_assertion wasGeneratedBy ECO_0000203 NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_provenance.