Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.
- NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_assertion description "[Defects in the human ALS2 gene, which encodes the 1,657-amino-acid residue protein alsin, are linked to several related motor neuron diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.
- NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_assertion evidence source_evidence_literature NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.
- NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_assertion SIO_000772 19023603 NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.
- NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_assertion wasDerivedFrom befree-2016 NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.
- NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_assertion wasGeneratedBy ECO_0000203 NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.
- befree-2016 importedOn "2016-02-19" NP704988.RAk8p-5vIsmo37rM_2NzC176bkbQolQOvXRrheAq-cWPw130_provenance.