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- NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_assertion type Assertion NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_head.
- NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_provenance.
- NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_assertion evidence source_evidence_literature NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_provenance.
- NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_assertion SIO_000772 23063620 NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_provenance.
- NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_assertion wasDerivedFrom befree-20150227 NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_provenance.
- NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_assertion wasGeneratedBy ECO_0000203 NP368254.RAHdiOSAvprwOLufryX4uHc0e8mIGx8NX2t3C2o-xSXBk130_provenance.