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- source_evidence_literature type ECO_0000212 NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.
- befree-2016 importedOn "2016-02-19" NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.
- NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_assertion wasGeneratedBy ECO_0000203 NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.
- NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_assertion wasDerivedFrom befree-2016 NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.
- NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_assertion SIO_000772 21844578 NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.
- NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_assertion evidence source_evidence_literature NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.
- NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_assertion description "[Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917313.RAcA5qTLL3dC7Cyxfx3JnhOPshTwZpleEkL8z2kcQFOxg130_provenance.