Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.
- NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_assertion description "[The -117(G-->A)A gamma hereditary persistence of fetal hemoglobin (Greek HPFH) and beta zero 39-thal mutations are rather frequent in Sardinia so that their interaction is to be expected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.
- NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_assertion evidence source_evidence_literature NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.
- NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_assertion SIO_000772 7543730 NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.
- NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_assertion wasDerivedFrom befree-2016 NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.
- NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_assertion wasGeneratedBy ECO_0000203 NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311792.RA3aOMiMYVnq1xCtKpRaYb-0Ko91FFV5GziO1znzSYFq0130_provenance.