Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.
- NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_assertion description "[RET/PTC1 (two out of seven) and RET/PTC3 (one out of seven), which have been shown in large PTC series to comprise together more than 90% of RET/PTC types, were found in <50% of the cases investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.
- NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_assertion evidence source_evidence_literature NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.
- NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_assertion SIO_000772 17464312 NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.
- NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_assertion wasDerivedFrom befree-20150227 NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.
- NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_assertion wasGeneratedBy ECO_0000203 NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788672.RASJlph3IgiI_PO5FYrJi-B4pKEUSAoRLI70ja3NqkT1A130_provenance.