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- source_evidence_literature type ECO_0000212 NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.
- NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_assertion description "[Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.
- NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_assertion evidence source_evidence_literature NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.
- NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_assertion SIO_000772 11978965 NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.
- NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_assertion wasDerivedFrom befree-20150227 NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.
- NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_assertion wasGeneratedBy ECO_0000203 NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964276.RAs6jNiz0H3y4nwl_VzKhsCLdDuqnnXcBF5TOBOLpTOWU130_provenance.