Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.
- NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_assertion wasGeneratedBy ECO_0000203 NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.
- NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_assertion wasDerivedFrom befree-20150227 NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.
- NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_assertion SIO_000772 21039331 NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.
- NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_assertion evidence source_evidence_literature NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.
- NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_assertion description "[Mutations in the gene cause a rare, recessive genetic disease, pseudoxanthoma elasticum, while the loss of one ABCC6 allele is a genetic risk factor in coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251255.RAKGtoCm-JKo87pSeVcKrZvTg6HHsrppTGAsjWvQ2cFXE130_provenance.