Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_assertion> ?p ?o ?g. }
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- NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_assertion type Assertion NP4036.RASTqhX_Im8oSqfyPI8jMJoMEMdKULY0bdKrDl7AtNSsg130_head.
- 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.