Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_assertion> ?p ?o ?g. }
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- NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_assertion type Assertion NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_head.
- NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_assertion wasGeneratedBy ECO_0000218 NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_provenance.
- NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_assertion wasDerivedFrom uniprot-2016 NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_provenance.
- NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_assertion SIO_000772 12927431 NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_provenance.
- NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_assertion evidence source_evidence_curated NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_provenance.
- NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_assertion description "[LMNA mutations in atypical Werner's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2831.RAgIzkYjPWnL4iMtXsMINW22JwsntL_-GBOX8-WHe1M0c130_provenance.