Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.
- NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_assertion description "[Niemann-Pick type C (NPC) disease is an autosomal recessive disorder caused by mutations of NPC1 and NPC2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.
- NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_assertion evidence source_evidence_literature NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.
- NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_assertion SIO_000772 17631520 NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.
- NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_assertion wasDerivedFrom befree-20140225 NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.
- NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_assertion wasGeneratedBy ECO_0000203 NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP289717.RAcCveZAx_pG4a_9xQfAJFWDMsnkw3fqNkTQ14RYN-k0I130_provenance.