Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.
- NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_assertion description "[Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.
- NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_assertion evidence source_evidence_literature NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.
- NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_assertion SIO_000772 22169395 NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.
- NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_assertion wasDerivedFrom befree-2016 NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.
- NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_assertion wasGeneratedBy ECO_0000203 NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.
- befree-2016 importedOn "2016-02-19" NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_provenance.