Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.
- NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_assertion description "[Mutations in GJB2, SLC26, TECTA and PJVK genes have an important role in HL in Iran and a screening test should be generated for better intervention and diagnosis programs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.
- NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_assertion evidence source_evidence_literature NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.
- NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_assertion SIO_000772 20739942 NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.
- NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_assertion wasDerivedFrom befree-20140225 NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.
- NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_assertion wasGeneratedBy ECO_0000203 NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP279861.RAdi5viaIeT0VpStKW4zsVOvEF_OG4esiRm5Ge4hGNvfY130_provenance.