Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.
- NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_assertion description "[Mutations of parkin, an E3 ubiquitin ligase that strongly binds to microtubules, are the most frequent cause of recessively inherited PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.
- NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_assertion evidence source_evidence_literature NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.
- NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_assertion SIO_000772 25332110 NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.
- NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_assertion wasDerivedFrom befree-2016 NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.
- NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_assertion wasGeneratedBy ECO_0000203 NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1230987.RA6HSZIK_8uI8D0iY7gHCukfTYbs1O_L5ss5z2YNcMtzE130_provenance.