Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_assertion> ?p ?o ?g. }
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- NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_assertion type Assertion NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_head.
- NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_assertion wasGeneratedBy ECO_0000203 NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_provenance.
- NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_assertion wasDerivedFrom befree-20150227 NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_provenance.
- NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_assertion SIO_000772 8028668 NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_provenance.
- NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_assertion evidence source_evidence_literature NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_provenance.
- NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_assertion description "[Sequence analysis revealed a striking identity (99%) of the subunit with a protein encoded by the causative gene (LIS-1) for Miller-Dieker lissencephaly, a human brain malformation manifested by a smooth cerebral surface and abnormal neuronal migration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606063.RA3IPpivOl-oqDexT-DRTejgqG7eM_n_aEmQvIoUYD7lk130_provenance.