Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_assertion evidence source_evidence_literature NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_assertion SIO_000772 18714162 NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_assertion wasDerivedFrom befree-20150227 NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_assertion wasGeneratedBy ECO_0000203 NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932810.RAyBPILfUa0sPJUN2cTOMoqbz4Y0NO8L6H9sA2-KgWEh4130_provenance.