Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_assertion> ?p ?o ?g. }
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- NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_assertion type Assertion NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_head.
- NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_assertion description "[MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_provenance.
- NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_assertion evidence source_evidence_literature NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_provenance.
- NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_assertion SIO_000772 17427193 NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_provenance.
- NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_assertion wasDerivedFrom gad-20150221 NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_provenance.
- NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_assertion wasGeneratedBy ECO_0000203 NP68885.RAgIc78EZHPoFgIYu0zMZmLqf4p9FGn-dCFru6zfuD-EM130_provenance.