Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.
- NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_assertion description "[The frequencies of the host genetic factors in the whole group were 0.52 for blood group O, 0.13 for hemoglobin S, 0.16 for the G6PD A-deficient variant and 0.24 for alpha+-thalassemia (-alpha(3.7) deletion).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.
- NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_assertion evidence source_evidence_literature NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.
- NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_assertion SIO_000772 16859949 NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.
- NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_assertion wasDerivedFrom befree-20140225 NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.
- NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_assertion wasGeneratedBy ECO_0000203 NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP243908.RA95RlQVEoMcwc1tSPWTSSkc3rlZeX81RUt4M08_cGSiI130_provenance.