Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.
- NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_assertion description "[Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.
- NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_assertion evidence source_evidence_literature NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.
- NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_assertion SIO_000772 16542389 NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.
- NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_assertion wasDerivedFrom befree-2016 NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.
- NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_assertion wasGeneratedBy ECO_0000203 NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.
- befree-2016 importedOn "2016-02-19" NP540692.RARKFjhv9kxsftlEp8j6UlTBdPdMyvmfzSwVEr7H9baW0130_provenance.