Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.
- NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_assertion description "[DCTN1 mutations, previously associated with motor neuron disease, can underlie the selective vulnerability of other neuronal populations in distinct neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.
- NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_assertion evidence source_evidence_literature NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.
- NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_assertion SIO_000772 19136952 NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.
- NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_assertion wasDerivedFrom lhgdn-20090331 NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.
- NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_assertion wasGeneratedBy ECO_0000203 NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP122058.RAQoPF06cBf86PNyjkrKh0PcbELLJOedgSD7U9hUnvg3w130_provenance.