Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_assertion evidence source_evidence_literature NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_assertion SIO_000772 23357145 NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_assertion wasDerivedFrom befree-20150227 NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_assertion wasGeneratedBy ECO_0000203 NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- befree-20150227 importedOn "2015-02-27" NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.