Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.
- NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_assertion description "[FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.
- NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_assertion evidence source_evidence_literature NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.
- NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_assertion SIO_000772 15956167 NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.
- NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_assertion wasDerivedFrom befree-20150227 NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.
- NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_assertion wasGeneratedBy ECO_0000203 NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412520.RAYkLmonS1akVj9BferUEl2bwr-QlEIjQp9GJFxe8rmPw130_provenance.