Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.
- NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_assertion description "[Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.
- NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_assertion evidence source_evidence_literature NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.
- NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_assertion SIO_000772 7994622 NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.
- NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_assertion wasDerivedFrom befree-20150227 NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.
- NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_assertion wasGeneratedBy ECO_0000203 NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443493.RA8u6_hLgC18hOLWSPxacVKdur6b3Rkuf-BEgOEf74F8g130_provenance.