Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.
- NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_assertion description "[Mutational analyses of NPHS1 and NPHS2 were performed to verify this hypothesis in sporadic nephrotic syndrome (NS) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.
- NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_assertion evidence source_evidence_literature NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.
- NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_assertion SIO_000772 17211152 NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.
- NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_assertion wasDerivedFrom befree-20150227 NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.
- NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_assertion wasGeneratedBy ECO_0000203 NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP783749.RAqFSO10yFdTQlAgvCwp2Kf9jKNnvYHO4K7c0-N_GuimU130_provenance.