Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.
- NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_assertion description "[Mice that carry null alleles for RET or for its ligand, glial cell line-derived neurotrophic factor (GDNF), both exhibit complete intestinal aganglionosis and renal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.
- NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_assertion evidence source_evidence_literature NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.
- NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_assertion SIO_000772 9881709 NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.
- NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_assertion wasDerivedFrom befree-2016 NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.
- NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_assertion wasGeneratedBy ECO_0000203 NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1412314.RAI1Y4rMgXCw5RRj0ynKq6XvpvifMMIY2kgznb-FUEIaw130_provenance.