Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.
- NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_assertion description "[Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.
- NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_assertion evidence source_evidence_literature NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.
- NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_assertion SIO_000772 22842229 NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.
- NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_assertion wasDerivedFrom befree-20150227 NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.
- NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_assertion wasGeneratedBy ECO_0000203 NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP939994.RAC0P1xsQb7ObSF24yazHw5L_fWsV-Spe1whNpTHlz-5Q130_provenance.