Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_assertion> ?p ?o ?g. }
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- NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_assertion type Assertion NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_head.
- NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_assertion description "[Homozygous disruption of PCP genes in mice results in a spectrum of NTDs, including defects that affect the entire neural axis (craniorachischisis), cranial NTDs (exencephaly) and spina bifida.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.
- NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_assertion evidence source_evidence_literature NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.
- NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_assertion SIO_000772 21840926 NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.
- NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_assertion wasDerivedFrom befree-20140225 NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.
- NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_assertion wasGeneratedBy ECO_0000203 NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.