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- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion type Assertion NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_head.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion description "[ZFHX1B mutations cause a complex developmental phenotype characterized by severe mental retardation (MR) and multiple congenital defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion evidence source_evidence_literature NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion SIO_000772 15006694 NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion wasDerivedFrom befree-20140225 NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.
- NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_assertion wasGeneratedBy ECO_0000203 NP841979.RAAhFTrzRlgIR_bDmoDxnxtD2mu51b8MJwvfL-qrtwWBo130_provenance.