Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_assertion> ?p ?o ?g. }
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- NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_assertion type Assertion NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_head.
- NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_assertion description "[A cohort of patients with MPZ gene mutations was identified in 13 centres of the Inherited Neuropathies Consortium - Rare Disease Clinical Research Consortium (INC-RDCRC) between 2009 and 2012 and at Wayne State University between 1996 and 2009.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_provenance.
- NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_assertion evidence source_evidence_literature NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_provenance.
- NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_assertion SIO_000772 26310628 NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_provenance.
- NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_assertion wasDerivedFrom befree-2016 NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_provenance.
- NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_assertion wasGeneratedBy ECO_0000203 NP1293243.RAQrZaVmkSkG7irfRzb9avRIE422KevG6NQlTg5djOeRY130_provenance.