Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_assertion> ?p ?o ?g. }
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- NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_assertion type Assertion NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_head.
- NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_assertion description "[A moderate increase in the number of PMP22 genes led to hypomyelination comparable to CMT1A, whereas high copy numbers of transgenic PMP22 resulted in phenotypes resembling more severe forms of hereditary motor and sensory neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_provenance.
- NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_assertion evidence source_evidence_literature NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_provenance.
- NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_assertion SIO_000772 10586249 NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_provenance.
- NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_assertion wasDerivedFrom befree-20150227 NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_provenance.
- NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_assertion wasGeneratedBy ECO_0000203 NP662198.RA4yEWVgUaR1DFkjctXhrjKDysBjBfvJ1MkeqzgcCRop4130_provenance.