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- source_evidence_literature type ECO_0000212 NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.
- NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_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." NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.
- NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_assertion evidence source_evidence_literature NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.
- NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_assertion SIO_000772 18266205 NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.
- NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_assertion wasDerivedFrom befree-2016 NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.
- NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_assertion wasGeneratedBy ECO_0000203 NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.
- befree-2016 importedOn "2016-02-19" NP654834.RA_6fMJC-u4EE2B3ZGB7sr_EUj5LXN947r51Y5xJZ4deo130_provenance.