Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.
- NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_assertion description "[SLC30A6 has been implicated in Alzheimer disease, so these fusion gene data could explain a report of spastic paraplegia and dementia cosegregating in a family with deletion of the final exon of SPAST.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.
- NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_assertion evidence source_evidence_literature NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.
- NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_assertion SIO_000772 25065914 NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.
- NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_assertion wasDerivedFrom befree-20150227 NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.
- NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_assertion wasGeneratedBy ECO_0000203 NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP920151.RA1qfqkXV3GJ-d04qfG2KI4Aa-W2VB3D4vTxEFfW6KrMU130_provenance.