Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_assertion> ?p ?o ?g. }
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- NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_assertion type Assertion NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_head.
- NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_assertion description "[Overall, this study shows that the I92V LITAF sequence variant would be a good candidate for a biomarker in the case of the CMT1A/HNPP disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_provenance.
- NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_assertion evidence source_evidence_literature NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_provenance.
- NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_assertion SIO_000772 25342198 NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_provenance.
- NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_assertion wasDerivedFrom befree-2016 NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_provenance.
- NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_assertion wasGeneratedBy ECO_0000203 NP1232248.RAz0GoW7NehYYYiKXRuM2XWF_fInTCNVSrE8xs3fejRW8130_provenance.