Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion description "[Patients with multiple endocrine neoplasia (MEN) type 2 with known RET gene mutations as well as those with other heritable disorders are candidates for PGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion evidence source_evidence_literature NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion SIO_000772 21550946 NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion wasDerivedFrom befree-2016 NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_assertion wasGeneratedBy ECO_0000203 NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.
- befree-2016 importedOn "2016-02-19" NP892384.RAExRSx3rFVlYF0e-8UUDMQOxLd6fc5YEhu5EJJvMUU7s130_provenance.