Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.
- NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_assertion description "[A molecular case report of autosomal dominant retinitis pigmentosa: RP1/RHO sequence variants in a Turkish family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.
- NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_assertion evidence source_evidence_literature NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.
- NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_assertion SIO_000772 22321012 NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.
- NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_assertion wasDerivedFrom befree-20140225 NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.
- NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_assertion wasGeneratedBy ECO_0000203 NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.
- befree-20140225 importedOn "2014-02-25" NP472894.RAG2D1q20bs7PJiMIGUs6texMwgo8nQ42Bq4EA1EExOms130_provenance.