Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.
- NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_assertion description "[A variety of previously unreported mutations in the coding region of the CHST6 gene are associated with type I MCD in a cohort of patients in southern India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.
- NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_assertion evidence source_evidence_literature NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.
- NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_assertion SIO_000772 14609920 NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.
- NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_assertion wasDerivedFrom befree-20140225 NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.
- NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_assertion wasGeneratedBy ECO_0000203 NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP426931.RADr9m2ml4C7vCJhuydRrjZWaFgBoIDuuX6HG60SOctR0130_provenance.