Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.
- NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion description "[Some of these gene products are specifically dedicated to B(12) transport, whereas others embrace additional roles, which explains the heterogeneity in the clinical picture of the many genetic disorders causing B(12) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.
- NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion evidence source_evidence_literature NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.
- NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion SIO_000772 22547309 NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.
- NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion wasDerivedFrom befree-20140225 NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.
- NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_assertion wasGeneratedBy ECO_0000203 NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP345735.RAPLK8UZA6ADLCYBc2mS4lT0MQ7DuG9QJFiWmIoRaH1MY130_provenance.