Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.
- NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_assertion description "[Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.
- NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_assertion evidence source_evidence_literature NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.
- NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_assertion SIO_000772 20930055 NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.
- NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_assertion wasDerivedFrom befree-20140225 NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.
- NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_assertion wasGeneratedBy ECO_0000203 NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP685874.RAw38FobwbBaw5QO91AzVzLnWfK7oQhUB02HI4_tvR44k130_provenance.