Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.
- NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_assertion description "[Methylmalonic aciduria and homocystinuria, cblC type (OMIM 277400), is the most common inborn error of vitamin B(12) (cobalamin) metabolism, with about 250 known cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.
- NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_assertion evidence source_evidence_literature NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.
- NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_assertion SIO_000772 16311595 NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.
- NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_assertion wasDerivedFrom befree-20140225 NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.
- NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_assertion wasGeneratedBy ECO_0000203 NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP789775.RAWVMeibMOs_f1Bm5x_IaceRSxS9LMv2kBg_6T94-ulHQ130_provenance.