Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_assertion> ?p ?o ?g. }
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- NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_assertion type Assertion NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_head.
- NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_assertion description "[Pelizaeus-Merzbacher disease is a rare, sex-linked recessive, dysmyelinating disease of the central nervous system that has been associated with mutations in the myelin proteolipid protein (PLP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_provenance.
- NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_assertion evidence source_evidence_literature NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_provenance.
- NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_assertion SIO_000772 7574457 NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_provenance.
- NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_assertion wasDerivedFrom befree-2016 NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_provenance.
- NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_assertion wasGeneratedBy ECO_0000203 NP1313060.RAY47DTBovU5wUqMD97bsd0mOPFNOBqEeTwqhUlFES6C4130_provenance.