Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.
- NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_assertion description "[We have identified a new point mutation, in the SCN4A gene, in a family with a hyperkalaemic periodic paralysis phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.
- NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_assertion evidence source_evidence_literature NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.
- NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_assertion SIO_000772 10366610 NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.
- NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_assertion wasDerivedFrom befree-20140225 NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.
- NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_assertion wasGeneratedBy ECO_0000203 NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718300.RASGviki7Eo8o3YUUCKQu9SwV6LtX6O3jKgYkxSQaAHn8130_provenance.