Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.
- NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_assertion description "[Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.
- NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_assertion evidence source_evidence_curated NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.
- NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_assertion SIO_000772 2479017 NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.
- NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_assertion wasDerivedFrom uniprot-2016 NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.
- NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_assertion wasGeneratedBy ECO_0000218 NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7890.RARlGem4vWXv-ZzXf3tN_ANf8NVuDRjg6jNrZiEzuLanU130_provenance.