Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.
- NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_assertion wasGeneratedBy ECO_0000203 NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.
- NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_assertion wasDerivedFrom befree-20140225 NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.
- NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_assertion SIO_000772 11951178 NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.
- NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_assertion evidence source_evidence_literature NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.
- NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_assertion description "[In addition, patients with sporadic amyotrophic lateral sclerosis who had a homozygous CNTF gene defect showed significantly earlier disease onset but did not show a significant difference in disease duration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.
- befree-20140225 importedOn "2014-02-25" NP631695.RAExltHdVJbBXUoCg9lg0dF574B-mKrgOIqsVOlewol84130_provenance.