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- NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_assertion type Assertion NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_head.
- NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_assertion wasGeneratedBy ECO_0000203 NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_provenance.
- NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_assertion wasDerivedFrom befree-20150227 NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_provenance.
- NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_assertion SIO_000772 22739344 NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_provenance.
- NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_assertion evidence source_evidence_literature NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_provenance.
- NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_assertion description "[We believe that the FOXG1 gene should be considered in severely mentally retarded patients (no speech-language) with severe acquired microcephaly (-4 to-6 SD) and few clinical features suggestive of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404315.RAA7NCnUKWTKu0a3G8vaCVAc1EX0hcv_KU04lbLIL3z2w130_provenance.