Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_assertion> ?p ?o ?g. }
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- NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_assertion type Assertion NP946605.RAgDvuyrqpz7s-ikr69bmnmThat2gNFcTzTLDRakRWJAw130_head.
- 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.