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- source_evidence_literature type ECO_0000212 NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.
- NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_assertion description "[This study enables us to estimate the frequency of the SPG3A mutations in France at 39% in families with young-onset autosomal dominant spastic paraplegia after exclusion of SPG4 cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.
- NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_assertion evidence source_evidence_literature NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.
- NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_assertion SIO_000772 15596607 NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.
- NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_assertion wasDerivedFrom befree-20150227 NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.
- NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_assertion wasGeneratedBy ECO_0000203 NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710065.RAUZR1-J8JCaxIL6lTyLnTj3w3iJQL_hUzUaj41niNg4Y130_provenance.