Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.
- NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_assertion description "[Giant axonal neuropathy (GAN) is an early-onset neurological disorder caused by mutations in the GAN gene (encoding for gigaxonin), which is predicted to be an E3 ligase adaptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.
- NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_assertion evidence source_evidence_literature NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.
- NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_assertion SIO_000772 23585478 NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.
- NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_assertion wasDerivedFrom befree-20150227 NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.
- NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_assertion wasGeneratedBy ECO_0000203 NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP790926.RAoVe1j8AJgQQq2KL3-nb4sGIdyB5lD4xaFBS41MBCkoA130_provenance.