Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.
- NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_assertion description "[Mutations in COX10 have previously been reported in a single family with tubulopathy and leukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.
- NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_assertion evidence source_evidence_literature NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.
- NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_assertion SIO_000772 12928484 NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.
- NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_assertion wasDerivedFrom befree-20140225 NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.
- NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_assertion wasGeneratedBy ECO_0000203 NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP904619.RAB3OMof1YZvJcu_29y7Pefj1ypswdv0Zcr_qSj2mHPSs130_provenance.