Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion wasGeneratedBy ECO_0000203 NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion wasDerivedFrom befree-20140225 NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion SIO_000772 17431911 NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion evidence source_evidence_literature NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion description "[Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.