Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion wasGeneratedBy ECO_0000203 NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion wasDerivedFrom befree-20150227 NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion SIO_000772 19139306 NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion evidence source_evidence_literature NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.