Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.
- NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_assertion wasGeneratedBy ECO_0000203 NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.
- NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_assertion wasDerivedFrom befree-20150227 NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.
- NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_assertion SIO_000772 10416973 NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.
- NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_assertion evidence source_evidence_literature NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.
- NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_assertion description "[Infantile neuronal ceroid lipofuscinosis (INCL) is a progressive neurodegenerative disorder in childhood which is caused by the deficiency of the lysosomal palmitoyl-protein thioesterase (PPT) encoded by the CLN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639373.RAKcqOJO8vYfm_lWkFXtv7A7zG0oJ_vANTV2piDVt83hM130_provenance.