Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.
- NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_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." NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.
- NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_assertion evidence source_evidence_literature NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.
- NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_assertion SIO_000772 14524000 NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.
- NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_assertion wasDerivedFrom befree-20140225 NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.
- NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_assertion wasGeneratedBy ECO_0000203 NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP555906.RAsWtDDYAncDRtk96G4V2gF48esJW_SzHTImrRySXFCsA130_provenance.