Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.
- NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_assertion wasGeneratedBy ECO_0000203 NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.
- NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_assertion wasDerivedFrom befree-2016 NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.
- NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_assertion SIO_000772 21039331 NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.
- NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_assertion evidence source_evidence_literature NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.
- NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_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." NP849489.RAB1M67Qh8FbaG5JkEmS-JUd8IuKMwqAykoJ6ascD9byQ130_provenance.