Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.
- NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_assertion description "[Haplotype analysis of XRCC1 Arg194Trp (C/T) and Arg399Gln (G/A) revealed that the frequency of the T-A haplotype was significantly higher in PC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.
- NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_assertion evidence source_evidence_literature NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.
- NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_assertion SIO_000772 17196815 NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.
- NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_assertion wasDerivedFrom befree-20140225 NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.
- NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_assertion wasGeneratedBy ECO_0000203 NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP506332.RAHVu8HoT2Vm4-ahtBSKvkEsDa9XDqhqA5HwDpb7R_Pzw130_provenance.