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- source_evidence_literature type ECO_0000212 NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.
- NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_assertion description "[To our knowledge, this is the first German EOAD patient without a Volga-German ancestry and a positive family history for dementia carries the mutation PSEN-2 N141I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.
- NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_assertion evidence source_evidence_literature NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.
- NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_assertion SIO_000772 19073399 NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.
- NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_assertion wasDerivedFrom befree-20150227 NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.
- NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_assertion wasGeneratedBy ECO_0000203 NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP651034.RALVt6pMcPQ-EAEngp4FHxqQFiJNnSAYcZ2cHNIBRYhxI130_provenance.