Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.
- NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_assertion description "[SQSTM1 mutations may play a role in the majority of familial Paget's disease of bone ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.
- NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_assertion evidence source_evidence_literature NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.
- NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_assertion SIO_000772 14584883 NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.
- NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_assertion wasDerivedFrom lhgdn-20090331 NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.
- NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_assertion wasGeneratedBy ECO_0000203 NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP141007.RAK_MOstFqepAJZJ_hDVhKkaTu6swu_o20VVBUn4vx6Us130_provenance.