Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.
- NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_assertion description "[Furthermore, detailed analysis of PXR1 has revealed that mutations in this gene are responsible for complementation group 2 of the peroxisome biogenesis disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.
- NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_assertion evidence source_evidence_literature NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.
- NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_assertion SIO_000772 8993569 NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.
- NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_assertion wasDerivedFrom befree-2016 NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.
- NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_assertion wasGeneratedBy ECO_0000203 NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1365575.RAiKLi5WQ3hWyBQumgEehuGAw9Tnxe414kbVs5BDqUavc130_provenance.