Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.
- befree-2016 importedOn "2016-02-19" NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.
- NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_assertion wasGeneratedBy ECO_0000203 NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.
- NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_assertion wasDerivedFrom befree-2016 NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.
- NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_assertion SIO_000772 11139250 NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.
- NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_assertion evidence source_evidence_literature NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.
- NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_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." NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_provenance.