Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_assertion description "[A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_assertion evidence source_evidence_literature NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_assertion SIO_000772 19061983 NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_assertion wasDerivedFrom befree-20150227 NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_assertion wasGeneratedBy ECO_0000203 NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP817317.RA-6DGMCCzGMJfeS26bpHLc3OP0tuGt2Yxaj6BsqVXt9w130_provenance.