Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.
- NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_assertion description "[Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.
- NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_assertion evidence source_evidence_literature NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.
- NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_assertion SIO_000772 16670177 NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.
- NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_assertion wasDerivedFrom befree-20150227 NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.
- NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_assertion wasGeneratedBy ECO_0000203 NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.
- befree-20150227 importedOn "2015-02-27" NP337397.RAXLBscnQluBX2Yo0G8608R3Jvwz3UaGstvLBuRKCO7ec130_provenance.