Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.
- NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_assertion description "[This report describes a patient with thalassemia intermedia-like phenotype born to normal parents in whom globin gene sequencing detected a novel abnormal hemoglobin (Hb) due to a T to A substitution at codon 60 of the beta-globin gene arising as a de novo mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.
- NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_assertion evidence source_evidence_literature NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.
- NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_assertion SIO_000772 1985702 NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.
- NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_assertion wasDerivedFrom befree-20140225 NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.
- NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_assertion wasGeneratedBy ECO_0000203 NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP731568.RAkHWyvCfxM9Z25p2lEoJo7QY_-CjJMCrQLxYkCx-VIlo130_provenance.