Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_assertion type Assertion NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_head.
- NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_assertion description "[L1CAM, therefore, harbours mutations leading to either MASA syndrome or HSAS, and might be frequently implicated in X-linked mental retardation with or without hydrocephalus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.
- NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_assertion evidence source_evidence_literature NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.
- NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_assertion SIO_000772 7920660 NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.
- NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_assertion wasDerivedFrom befree-20150227 NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.
- NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_assertion wasGeneratedBy ECO_0000203 NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.