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- source_evidence_literature type ECO_0000212 NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.
- NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_assertion description "[Furthermore, AT-1 defects are a new and important differential diagnosis in patients with low copper and ceruloplasmin in serum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.
- NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_assertion evidence source_evidence_literature NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.
- NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_assertion SIO_000772 22243965 NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.
- NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_assertion wasDerivedFrom befree-2016 NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.
- NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_assertion wasGeneratedBy ECO_0000203 NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.
- befree-2016 importedOn "2016-02-19" NP953104.RAEePw04Qyjr16h7J4xrauDovBekz0POWpesXxmovT5hk130_provenance.