Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.
- NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_assertion description "[Sequence variations or mutations of one single gene, coding for the host regulator Factor H, form the basis for multiple, different disorders such as human renal and retinal diseases as well as infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.
- NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_assertion evidence source_evidence_literature NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.
- NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_assertion SIO_000772 19388168 NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.
- NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_assertion wasDerivedFrom befree-20150227 NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.
- NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_assertion wasGeneratedBy ECO_0000203 NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446373.RAh5dfxV0BrHchRH-zqDVNjBPITP2GsRzG4leZHM8a9QY130_provenance.