Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.
- NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_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." NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.
- NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_assertion evidence source_evidence_literature NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.
- NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_assertion SIO_000772 20181727 NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.
- NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_assertion wasDerivedFrom befree-2016 NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.
- NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_assertion wasGeneratedBy ECO_0000203 NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.
- befree-2016 importedOn "2016-02-19" NP795882.RAbdHAVXaM9Os8vTKegadL39dBQEi_THw3iG2wqShS55k130_provenance.