Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.
- NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_assertion description "[Only 12 of the 43 patients with an abnormal fluorometric screening test were found to have less than 3% GALT activity by quantitative assay, no GALT-staining by IEF, and a clinical history consistent with classical galactosemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.
- NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_assertion evidence source_evidence_literature NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.
- NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_assertion SIO_000772 2546999 NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.
- NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_assertion wasDerivedFrom befree-2016 NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.
- NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_assertion wasGeneratedBy ECO_0000203 NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244396.RAPBjg3IiReex3td5Z9N-Vr43Mm1oXpTI3cAnr7a8h0PU130_provenance.