Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.
- NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion description "[To understand the role of hemochromatosis and transferrin receptor system mutations in breast cancer, we analyzed 19 sequence variations at HFE, TFR1, TFR2, and FPN1 and compared genotype frequencies between cases and controls in a German population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.
- NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion evidence source_evidence_literature NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.
- NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion SIO_000772 15894659 NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.
- NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion wasDerivedFrom befree-20140225 NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.
- NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_assertion wasGeneratedBy ECO_0000203 NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP683884.RAzTX2Ua44696zWVrQ-GQRt9YjrEdgjEp9LX-Ot-DHoSs130_provenance.