Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.
- NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_assertion wasGeneratedBy ECO_0000203 NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.
- NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_assertion wasDerivedFrom befree-20140225 NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.
- NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_assertion SIO_000772 17003072 NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.
- NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_assertion evidence source_evidence_literature NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.
- NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_assertion description "[Niemann-Pick disease type C (NPC) is a fatal neurovisceral lipid storage disease of autosomal inheritance resulting from mutations in either the NPC1 (95% of families) or NPC2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP636079.RAn3B1HyjFiu5YfuG1vg6J5HUpJgLRGYxoXoFzGs2zZ7w130_provenance.