Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.
- NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_assertion description "[The region mutated in Liddle syndrome, called the PY motif (L/PPxY), serves as a binding site for the ubiquitin ligase Nedd4-2, a C2-WW-Hect E3 ubiquitin ligase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.
- NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_assertion evidence source_evidence_literature NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.
- NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_assertion SIO_000772 18691017 NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.
- NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_assertion wasDerivedFrom befree-20140225 NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.
- NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_assertion wasGeneratedBy ECO_0000203 NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900643.RAM0Y7nzjyTb-WSBHOzDkdySeSLIDR8E8_CPyQ-g0fUTs130_provenance.