Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.
- NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_assertion description "[We have previously characterized mutant adenosine deaminase (ADA; adenosine aminohydrolase, EC 3.5.4.4) enzymes in seven children with partial ADA deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.
- NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_assertion evidence source_evidence_literature NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.
- NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_assertion SIO_000772 2166947 NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.
- NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_assertion wasDerivedFrom befree-20150227 NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.
- NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_assertion wasGeneratedBy ECO_0000203 NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP908795.RAy2lgW0Mn7MjZqTvHoRI_d_63xPFrbobT1wQ9nRk9KbQ130_provenance.