Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_assertion> ?p ?o ?g. }
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- NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_assertion type Assertion NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_head.
- NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_assertion wasGeneratedBy ECO_0000203 NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_provenance.
- NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_assertion wasDerivedFrom befree-2016 NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_provenance.
- NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_assertion SIO_000772 22490426 NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_provenance.
- NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_assertion evidence source_evidence_literature NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_provenance.
- NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_assertion description "[Pelizaeus-Merzbacher disease (PMD; MIM#312080) is a rare X-linked leukodystrophy presenting with motor developmental delay associated with spasticity and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP973678.RAPJwymOFFRhJRzfFq0BNss7Klaobb8RqomDhO7TuFYiQ130_provenance.