Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.
- NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_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." NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.
- NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_assertion evidence source_evidence_literature NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.
- NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_assertion SIO_000772 21840926 NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.
- NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_assertion wasDerivedFrom befree-20140225 NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.
- NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_assertion wasGeneratedBy ECO_0000203 NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.
- befree-20140225 importedOn "2014-02-25" NP407100.RAik9qpncFIDGrJtkL-RJaNzHwqn2VTgRMcheMx5p-j78130_provenance.