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- source_evidence_literature type ECO_0000212 NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_assertion description "[Megaloblastic anaemia 1 (MGA1, OMIM 261100) is a rare, autosomal recessive disorder characterized by juvenile megaloblastic anaemia, as well as neurological symptoms that may be the only manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_assertion evidence source_evidence_literature NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_assertion SIO_000772 10080186 NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_assertion wasDerivedFrom befree-20150227 NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_assertion wasGeneratedBy ECO_0000203 NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788378.RA3W3rCCR3lY76jexqWcOpj7OGeF0-Igi8aol9RnYsJT4130_provenance.