Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.
- NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_assertion description "[In conclusion, our data show for the first time a high prevalence of AR gene mutations in patients affected by TC and suggest that some CAG/GGC combinations might be more frequently associated with an increased risk of TC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.
- NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_assertion evidence source_evidence_literature NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.
- NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_assertion SIO_000772 16172197 NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.
- NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_assertion wasDerivedFrom befree-20150227 NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.
- NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_assertion wasGeneratedBy ECO_0000203 NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP941897.RAauI7YcVcdci-r2KTlwA2n57OHxQ7azbQENODCvB-AyI130_provenance.