Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.
- NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_assertion description "[Novel point mutation of the ?2-globin gene (HBA2) and a rare 2.4?kb deletion of the ?1-globin gene (HBA1), identified in two chinese patients with Hb H disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.
- NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_assertion evidence source_evidence_literature NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.
- NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_assertion SIO_000772 24826793 NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.
- NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_assertion wasDerivedFrom befree-20150227 NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.
- NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_assertion wasGeneratedBy ECO_0000203 NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443542.RAZ_ISSUmE1qhoSSXoHVdnR2kQ2-h8chGud8Bt5L7k7FE130_provenance.