Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.
- NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_assertion description "[The mother has patchy fundal hypopigmentation consistent with random X inactivation in an OA1 carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.
- NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_assertion evidence source_evidence_literature NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.
- NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_assertion SIO_000772 2573275 NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.
- NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_assertion wasDerivedFrom befree-20140225 NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.
- NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_assertion wasGeneratedBy ECO_0000203 NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP452644.RAr5X5dF19sxt-tRHq0ulJELEd3vjobUydFEwe82N5SzE130_provenance.