Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.
- NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_assertion description "[As far as we know, the present study has shown the highest frequency of 21OHD carriers reported by a genotyping analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.
- NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_assertion evidence source_evidence_literature NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.
- NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_assertion SIO_000772 18478071 NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.
- NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_assertion wasDerivedFrom gad-20150221 NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.
- NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_assertion wasGeneratedBy ECO_0000203 NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123041.RAc0p6Vzj-De2GgeKxjp9zaXlQZ98gSeaBRu9WgH32Hdw130_provenance.