Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.
- NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_assertion description "[The protein sacsin, which is mutated in the early-onset neurodegenerative disease autosomal recessive spastic ataxia of Charlevoix-Saguenay, is a node in this interactome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.
- NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_assertion evidence source_evidence_literature NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.
- NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_assertion SIO_000772 19208651 NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.
- NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_assertion wasDerivedFrom befree-20140225 NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.
- NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_assertion wasGeneratedBy ECO_0000203 NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP614265.RAIqWWOheQPcVbC0xCUSZ53y7ppssrhnp2wnjIdff15tU130_provenance.