Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_assertion type Assertion NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_head.
- NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_assertion description "[We investigated the proteolipid protein (PLP) gene of two boys in a Japanese family with Pelizaeus-Merzbacher disease (PMD), an X-linked neurologic disorder characterized by dysmyelination in the central nervous system (CNS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_provenance.
- NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_assertion evidence source_evidence_literature NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_provenance.
- NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_assertion SIO_000772 7683951 NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_provenance.
- NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_assertion wasDerivedFrom befree-2016 NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_provenance.
- NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_assertion wasGeneratedBy ECO_0000203 NP1318065.RAbRy7mPS6-47hN1AagHw0l6cdBPuJGO5w5iBZEjVTrR0130_provenance.