Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.
- NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_assertion description "[Mutations in the MMAA gene on human chromosome 4q31.21 result in vitamin B12-responsive methylmalonic aciduria (cblA complementation group) due to deficiency in the synthesis of adenosylcobalamin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.
- NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_assertion evidence source_evidence_literature NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.
- NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_assertion SIO_000772 15523652 NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.
- NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_assertion wasDerivedFrom befree-20150227 NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.
- NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_assertion wasGeneratedBy ECO_0000203 NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977649.RAoMa2UhEAoKvqNOeJMVe9op6_kRAN_XRpVnx26Jo01bQ130_provenance.