Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_assertion type Assertion NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_head.
- NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_assertion description "[The relatively low observed frequency of MECP2 mutations reflects a wide spectrum of mental disability disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_provenance.
- NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_assertion evidence source_evidence_literature NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_provenance.
- NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_assertion SIO_000772 19652677 NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_provenance.
- NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_assertion wasDerivedFrom befree-20140225 NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_provenance.
- NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_assertion wasGeneratedBy ECO_0000203 NP629512.RABBSuBunKMMbH0BHgkHbAsQJIn8M7IWueEbOtYCo0uQI130_provenance.