Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.
- NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_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." NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.
- NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_assertion evidence source_evidence_literature NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.
- NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_assertion SIO_000772 22547309 NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.
- NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_assertion wasDerivedFrom befree-20140225 NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.
- NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_assertion wasGeneratedBy ECO_0000203 NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP486974.RAW-YazoO7H_E3EzNCR88OoQIIbg7Lj8vcSYj1whMcwJA130_provenance.