Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.
- NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_assertion description "[Among 20 p deletions tested, there was complete concordance between alterations at the Gabrb3 transcription unit and inability to complement the cleft-palate defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.
- NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_assertion evidence source_evidence_literature NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.
- NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_assertion SIO_000772 8389469 NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.
- NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_assertion wasDerivedFrom befree-2016 NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.
- NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_assertion wasGeneratedBy ECO_0000203 NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1340289.RAR3EPdYNx2M_dPRJTefwqEiFVz4LbFXH0SiLJEpl_smY130_provenance.