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- NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_assertion type Assertion NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_head.
- NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_assertion wasGeneratedBy ECO_0000203 NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_provenance.
- NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_assertion wasDerivedFrom befree-20140225 NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_provenance.
- NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_assertion SIO_000772 10430413 NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_provenance.
- NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_assertion evidence source_evidence_literature NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_provenance.
- NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_assertion description "[We compared the phenotype, especially brain imaging studies, in a series of 48 children with lissencephaly, including 12 with Miller-Dieker syndrome (MDS), which is associated with large deletions of LIS1 and other genes in the region, 24 with isolated lissencephaly sequence caused by smaller LIS1 deletions or mutations, and 12 with isolated lissencephaly sequence caused by XLIS mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466350.RAVzs-yEQTRf42Ly8JbcBAVWsFhPF56nEHKr1Bs1Kao5E130_provenance.