Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_assertion evidence source_evidence_literature NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_assertion SIO_000772 11439091 NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_assertion wasDerivedFrom befree-20140225 NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_assertion wasGeneratedBy ECO_0000203 NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP893023.RAtwLI4EH1Vqr5u0jdk9oVzz8_UIuct2SKFgiPb0Rw42U130_provenance.