Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_assertion type Assertion NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_head.
- NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_assertion wasGeneratedBy ECO_0000203 NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_provenance.
- NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_assertion wasDerivedFrom befree-2016 NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_provenance.
- NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_assertion SIO_000772 12719401 NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_provenance.
- NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_assertion evidence source_evidence_literature NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_provenance.
- NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_assertion description "[Neonatal encephalopathy in males is part of a spectrum of disorders caused by MECP2 dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392606.RApyc29tLJRo_NF2VAEhEvhCljVHbzvuB_57K3oMLFQCc130_provenance.