Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_assertion> ?p ?o ?g. }
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- NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_assertion type Assertion NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_head.
- NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_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." NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_provenance.
- NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_assertion evidence source_evidence_literature NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_provenance.
- NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_assertion SIO_000772 16859949 NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_provenance.
- NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_assertion wasDerivedFrom befree-2016 NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_provenance.
- NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_assertion wasGeneratedBy ECO_0000203 NP560803.RAj2RuGElajbYKSyl1h1_qXeizeVrnF5SRCKxjCi_HN-Y130_provenance.