Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.
- NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_assertion wasGeneratedBy ECO_0000203 NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.
- NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_assertion wasDerivedFrom befree-20140225 NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.
- NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_assertion SIO_000772 11565064 NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.
- NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_assertion evidence source_evidence_literature NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.
- NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_assertion description "[The results show that mutations in COL9A1 can cause MED, but they also suggest that mutations in COL9A1, COL9A2, COL9A3, COMP, and DTDST are not the major causes of MED and that there exists at least one additional locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP402407.RA4L0oAj5vj9Cfx9tfRySPhjbqXxv3KJlX-c7CJo9nKfs130_provenance.