Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.
- NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_assertion description "[That in this population second mutations producing G6PD deficiency occurred only on the genetic background of G6PD A suggests that G6PD A was at one time the most common type of G6PD in Africa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.
- NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_assertion evidence source_evidence_literature NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.
- NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_assertion SIO_000772 2572288 NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.
- NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_assertion wasDerivedFrom befree-2016 NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.
- NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_assertion wasGeneratedBy ECO_0000203 NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266714.RAUJLfLnkIvMLyiru3oLw2RaZ-eWUiYD8tzgW82_BOHSE130_provenance.