Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.
- befree-2016 importedOn "2016-02-19" NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.
- NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_assertion wasGeneratedBy ECO_0000203 NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.
- NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_assertion wasDerivedFrom befree-2016 NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.
- NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_assertion SIO_000772 17855450 NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.
- NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_assertion evidence source_evidence_literature NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.
- NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_assertion description "[Mutations in Alsin are associated with chronic juvenile amyotrophic lateral sclerosis (ALS2), juvenile primary lateral sclerosis and infantile-onset ascending spastic paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629982.RAcszH5ueZDY12izvI0J8mQ7L7TL6r9Rap2egm2IQEryE130_provenance.