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- NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_assertion type Assertion NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_head.
- NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_assertion description "[DCX mutations are responsible for almost all familial cases, 80% of sporadic female cases, and 25% of sporadic male cases of SBH, and are associated with more severe gyral and migration abnormality over the anterior brain regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_provenance.
- NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_assertion evidence source_evidence_literature NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_provenance.
- NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_assertion SIO_000772 14581661 NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_provenance.
- NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_assertion wasDerivedFrom befree-2016 NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_provenance.
- NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_assertion wasGeneratedBy ECO_0000203 NP418446.RAXs7Kw_Fs3fbUQlUYfT03ZRY0xv_qUpn91LPj_jAIUf8130_provenance.