Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.
- befree-2016 importedOn "2016-02-19" NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.
- NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_assertion wasGeneratedBy ECO_0000203 NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.
- NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_assertion wasDerivedFrom befree-2016 NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.
- NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_assertion SIO_000772 20584796 NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.
- NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_assertion evidence source_evidence_literature NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.
- NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_assertion description "[Congenital defects of genes known to disturb surfactant protein and lipid homeostasis (SFTPB, SFTPC, ABCA3) were excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822073.RAmn1cw0JoX3oPHqgNcUAtMife8EClrw0AQ1fjFCJ9I4o130_provenance.