Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP530058.RAXhKiJTXWFIahsIm3bd0XkcGjb68BkXOe8wd1GMJwD1I130_provenance.