Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_assertion> ?p ?o ?g. }
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- NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_assertion type Assertion NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_head.
- NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_assertion wasGeneratedBy ECO_0000203 NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_provenance.
- NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_assertion wasDerivedFrom befree-2016 NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_provenance.
- NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_assertion SIO_000772 8028668 NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_provenance.
- NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_assertion evidence source_evidence_literature NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_provenance.
- NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_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." NP1330267.RAbbqMDnYSHf5wn7xootWiUYaxWg2-32Vf3LlW-UafBa0130_provenance.