Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.
- NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_assertion description "[Among the congenital sideroblastic anemias (CSAs), the most common form is X-linked sideroblastic anemia, due to mutations in 5-aminolevulinate synthase (ALAS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.
- NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_assertion evidence source_evidence_literature NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.
- NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_assertion SIO_000772 19731322 NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.
- NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_assertion wasDerivedFrom befree-20140225 NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.
- NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_assertion wasGeneratedBy ECO_0000203 NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP679780.RASMhdQgbFOA1YJqswxpnGaimZ1hlGg6Z4CvoterFmxTM130_provenance.