Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.
- NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_assertion description "[The majority of evaluations (43 of 59) were undertaken because of an abnormal fluorometric GALT screening assay conducted as part of a state newborn galactosemia screening program or as a diagnostic test for an infant with one or more clinical signs of galactosemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.
- NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_assertion evidence source_evidence_literature NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.
- NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_assertion SIO_000772 2546999 NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.
- NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_assertion wasDerivedFrom befree-2016 NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.
- NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_assertion wasGeneratedBy ECO_0000203 NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244397.RAa1bDJHcj9EDg4h0M3o0bZ1iqxIPm5Pm2_M6GzlxIl8o130_provenance.