Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_assertion> ?p ?o ?g. }
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- NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_assertion type Assertion NP304363.RAFvcZT97rUWfIQ8PRNQtT4sH2x7geDG9IB_ziXqFKnP4130_head.
- 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.