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- source_evidence_literature type ECO_0000212 NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.
- NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_assertion description "[Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.
- NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_assertion evidence source_evidence_literature NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.
- NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_assertion SIO_000772 22560297 NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.
- NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_assertion wasDerivedFrom befree-20140225 NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.
- NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_assertion wasGeneratedBy ECO_0000203 NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651758.RAZSwoL3Z4OkVrd-ir3UZ2WUaQSxGxTmyi22sQ7pXQne8130_provenance.