Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.
- NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_assertion description "[A mutation in the 3'-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.
- NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_assertion evidence source_evidence_literature NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.
- NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_assertion SIO_000772 20181727 NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.
- NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_assertion wasDerivedFrom befree-20150227 NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.
- NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_assertion wasGeneratedBy ECO_0000203 NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1003582.RAlVoUwXyz6kg6mTD3g5aPVICoMnwp-8bNYztTJENSkB0130_provenance.