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- source_evidence_literature type ECO_0000212 NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.
- NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion description "[Based on the InSiGHT database and the original references that reported the mutations, we analyzed the distributions of MLH1 and MSH2 mutations in yellow race and white race respectively and compared them subsequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.
- NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion evidence source_evidence_literature NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.
- NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion SIO_000772 21155023 NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.
- NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion wasDerivedFrom befree-20140225 NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.
- NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion wasGeneratedBy ECO_0000203 NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance.