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- source_evidence_literature type ECO_0000212 NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_assertion description "[Mutations in the MTR gene, which encodes methionine synthase on human chromosome 1p43, result in the methylcobalamin deficiency G (cblG) disorder, which is characterized by homocystinuria, hyperhomocysteinemia, and hypomethioninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_assertion evidence source_evidence_literature NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_assertion SIO_000772 12068375 NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_assertion wasDerivedFrom befree-20150227 NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_assertion wasGeneratedBy ECO_0000203 NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.