Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.
- NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_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." NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.
- NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_assertion evidence source_evidence_literature NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.
- NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_assertion SIO_000772 19388168 NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.
- NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_assertion wasDerivedFrom befree-2016 NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.
- NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_assertion wasGeneratedBy ECO_0000203 NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.
- befree-2016 importedOn "2016-02-19" NP734267.RA33KcL4K7bBDMheklwGeNNWmRJfNbsA2h8JeEFQnR17c130_provenance.