Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.
- NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_assertion description "[Mutations in SLC6A5, encoding GlyT2, cause hereditary hyperekplexia in humans, and similar phenotypes in knock-out mice, and variants are associated with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.
- NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_assertion evidence source_evidence_literature NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.
- NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_assertion SIO_000772 22272310 NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.
- NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_assertion wasDerivedFrom befree-20150227 NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.
- NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_assertion wasGeneratedBy ECO_0000203 NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP816169.RAjMmLKTGsZt3AIi_QsthLLWAulUBzrrsKHlUwyeI65UU130_provenance.