Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.
- NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_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." NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.
- NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_assertion evidence source_evidence_literature NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.
- NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_assertion SIO_000772 22842229 NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.
- NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_assertion wasDerivedFrom befree-20140225 NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.
- NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_assertion wasGeneratedBy ECO_0000203 NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449185.RAV823lYlYg3-ekjEy4hC6WBSvDL_5np5vHcTb2Q6GN3E130_provenance.