Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_assertion wasGeneratedBy ECO_0000203 NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_assertion wasDerivedFrom befree-20140225 NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_assertion SIO_000772 19139306 NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_assertion evidence source_evidence_literature NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_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." NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.