Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.
- NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_assertion description "[A novel COL4A5 mutation causes rapid progression to end-stage renal disease in males, despite the absence of clinical and biopsy findings associated with Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.
- NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_assertion evidence source_evidence_literature NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.
- NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_assertion SIO_000772 20881942 NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.
- NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_assertion wasDerivedFrom befree-20140225 NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.
- NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_assertion wasGeneratedBy ECO_0000203 NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP851620.RAsBTQmrVU7uCQQN-5W5Lx9UlNY3o6PA5zfrdcoUXJvf4130_provenance.