Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP714125.RAuYu0ukt02imXenIIZGEcE3i1SfQ0eeATnxG1DdLgfz0130_provenance.