Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.
- NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_assertion description "[OCA3 (MIM 203290), a rare form of OCA and also known as rufous/red albinism, is associated with mutations in TYRP1 (encoding tyrosinase-related protein 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.
- NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_assertion evidence source_evidence_literature NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.
- NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_assertion SIO_000772 11574907 NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.
- NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_assertion wasDerivedFrom befree-2016 NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.
- NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_assertion wasGeneratedBy ECO_0000203 NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.
- befree-2016 importedOn "2016-02-19" NP331296.RAoIxmy9XZLxtx94pDFF6ygG5IEfL_sP2FiAq1SzIgrP0130_provenance.