Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.
- NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_assertion wasGeneratedBy ECO_0000218 NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.
- NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_assertion wasDerivedFrom uniprot-20130724 NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.
- NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_assertion SIO_000772 19201763 NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.
- NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_assertion evidence source_evidence_curated NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.
- NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_assertion description "[Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_provenance.