Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion description "[Of these 12 patients, three had homozygous G701D/G701D and heterozygous Hb E; one compound heterozygous SAO/G701D and heterozygous alpha(+)-thalassemia; and one compound heterozygous G701D/A858D and heterozygous Hb E. Of 6 patients without SLC4A1 mutation, two each carried heterozygous or homozygous Hb E and one of the latter also had Hb H disease (--(SEA)/-alpha(4.2)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion evidence source_evidence_literature NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion SIO_000772 18266205 NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion wasDerivedFrom befree-20140225 NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_assertion wasGeneratedBy ECO_0000203 NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP665718.RAuh_6bZUb0nGFxHC9W6Dw5U_93TpJwC-Oka2zWpb020U130_provenance.