Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.
- NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_assertion description "[In this study, we used new molecular and genomic data generated from four HapMap population samples to test the idea that positive selection for an as-of-yet unknown fitness benefit of the RHD deletion may have offset the otherwise negative fitness effects of hemolytic disease of the newborn.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.
- NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_assertion evidence source_evidence_literature NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.
- NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_assertion SIO_000772 22367406 NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.
- NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_assertion wasDerivedFrom befree-20140225 NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.
- NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_assertion wasGeneratedBy ECO_0000203 NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP446538.RAAxpWZm_e_46ebp1ieVXothgebKsPu1RX50w7c1zgdoU130_provenance.