Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.
- NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_assertion description "[A genetic mutation within its MSP domain, P56S, was identified in familial forms of motor neuron diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.
- NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_assertion evidence source_evidence_literature NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.
- NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_assertion SIO_000772 20207736 NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.
- NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_assertion wasDerivedFrom befree-20140225 NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.
- NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_assertion wasGeneratedBy ECO_0000203 NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP707389.RAe5CZ9vPewROvkXg6_weguUHZC_CO-Q-maQqLw-qLp0w130_provenance.