Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_assertion> ?p ?o ?g. }
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- NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_assertion type Assertion NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_head.
- NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_assertion description "[A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_provenance.
- NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_assertion evidence source_evidence_curated NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_provenance.
- NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_assertion SIO_000772 19559301 NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_provenance.
- NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_assertion wasDerivedFrom ctd_human-20150221 NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_provenance.
- NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_assertion wasGeneratedBy ECO_0000218 NP21799.RAkP7NdTuYcWW6a0JtZHmAbWxR10mKi6eRZE8WdeGFkg4130_provenance.