Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.
- NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_assertion wasGeneratedBy ECO_0000203 NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.
- NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_assertion wasDerivedFrom befree-20150227 NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.
- NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_assertion SIO_000772 22387303 NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.
- NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_assertion evidence source_evidence_literature NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.
- NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_assertion description "[Infantile neuronal ceroid lipofuscinosis (INCL; NCL1, Haltia-Santavuori disease) is caused by mutations in the CLN1/PPT gene which are associated with an early onset INCL phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639407.RAmxY1F6_EFcCOgIZ-fDgJY8__MLzSYwHSrA-9zgyIDKw130_provenance.