Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.
- NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_assertion description "[The phenotype and allele frequencies of the four gene loci (AB0, RH, PTC and colour blindness) show considerable differences between these populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.
- NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_assertion evidence source_evidence_literature NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.
- NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_assertion SIO_000772 14524000 NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.
- NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_assertion wasDerivedFrom befree-20150227 NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.
- NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_assertion wasGeneratedBy ECO_0000203 NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788557.RAfBdKcfjOoCRmCoFpn8b7zdVG9ZInaP1PGHcAe_8G9Cw130_provenance.