Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.
- NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_assertion description "[Three genetic forms of FHBL exist: (a) FHBL caused by truncation-specifying mutations of apolipoprotein B (apoB), (b) FHBL linked to chr3p21, and (c) FHBL not linked either to APOB or to chr3p21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.
- NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_assertion evidence source_evidence_literature NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.
- NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_assertion SIO_000772 15877300 NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.
- NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_assertion wasDerivedFrom befree-20140225 NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.
- NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_assertion wasGeneratedBy ECO_0000203 NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP166327.RAKgzyIFv-59KMo4gCEcwZMf6K2Njip31CmSXMWvusXsM130_provenance.