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- source_evidence_literature type ECO_0000212 NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.
- NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_assertion description "[It seems likely that this technology will also have an impact on the management of sporadic MTC, although it is still too early to define a specific role for mutational analysis in these patients, except to exclude hereditary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.
- NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_assertion evidence source_evidence_literature NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.
- NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_assertion SIO_000772 7575334 NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.
- NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_assertion wasDerivedFrom befree-20150227 NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.
- NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_assertion wasGeneratedBy ECO_0000203 NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP571879.RAEh0-0SXvOjWwy_1PRTWfCu-as40FxqRl3s0UNnxi1lA130_provenance.