Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion> ?p ?o ?g. }
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- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion type Assertion NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_head.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion description "[Linkage to 1p35-p36 (CMT2A), 3q (CMT2B), and 7p (CMT2D) chromosomes has been reported in the disease; however, most HMSN II families do not link to any of the reported loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion evidence source_evidence_literature NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion SIO_000772 9595994 NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion wasDerivedFrom befree-20140225 NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.
- NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_assertion wasGeneratedBy ECO_0000203 NP766378.RANOMWXJ2OxAPFbUYsUPYsX7u4YF52ledhx2K8cWM874I130_provenance.