Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.
- NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_assertion description "[Mutations of the RET, GFRA1, PHOX2A, and HASH-1 genes may also be involved in the pathogenesis of CCHS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.
- NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_assertion evidence source_evidence_literature NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.
- NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_assertion SIO_000772 14566559 NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.
- NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_assertion wasDerivedFrom befree-20140225 NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.
- NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_assertion wasGeneratedBy ECO_0000203 NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.
- befree-20140225 importedOn "2014-02-25" NP251680.RAk2LtUgNBtAX6xZ4A6GxRVA2PUsjG1iJCvFt_wS8a2Ps130_provenance.