Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_assertion wasGeneratedBy ECO_0000203 NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_assertion wasDerivedFrom befree-20140225 NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_assertion SIO_000772 11139250 NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_assertion evidence source_evidence_literature NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_assertion description "[Our data exclude the responsibility of the pM5, MRP1 and NPIP genes in PXE, and strongly suggest that mutations in the last remaining candidate gene, MRP6, which encodes a 1503 amino-acid ABC membrane transporter, are the genetic defect responsible for PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP416924.RALHt1qePeoJZ6RtkPD-DrcwiMEKKfummKF0cnclMEqXw130_provenance.