Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.
- NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion description "[A comparison of several statistical methods and measures (gene frequency, haplotype frequency, and linkage disequilibrium estimation) using the Centre d'Etude du Polymorphisme Humain data will be provided using KIR haplotypes that have been determined by segregation analysis, noting the strengths and weaknesses of the methods when only the presence/absence data is considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.
- NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion evidence source_evidence_literature NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.
- NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion SIO_000772 18797862 NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.
- NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion wasDerivedFrom befree-20140225 NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.
- NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_assertion wasGeneratedBy ECO_0000203 NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624961.RAytazkIIdD-7srv2cnZMtT_P81ZtMxNFZyhS3iZkzNPg130_provenance.