Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.
- NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_assertion wasGeneratedBy ECO_0000203 NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.
- NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_assertion wasDerivedFrom befree-20140225 NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.
- NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_assertion SIO_000772 21965087 NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.
- NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_assertion evidence source_evidence_literature NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.
- NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_assertion description "[Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP346298.RAWbfe_lQ7pm5zZzVE5Vz6fvqal6L7v1Gr1TBKIuOFZmI130_provenance.