Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.
- NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_assertion description "[We used genomic DNA of 48 patients with focal segmental glomerulosclerosis (FSGS) and minimal change disease (MCD) to screen for ACTN4 mutations by high-resolution melting analysis (HRM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.
- NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_assertion evidence source_evidence_literature NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.
- NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_assertion SIO_000772 23890478 NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.
- NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_assertion wasDerivedFrom befree-2016 NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.
- NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_assertion wasGeneratedBy ECO_0000203 NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1097241.RApmo4KyuqlQTgfQYZ0-Uc6-mtIYg_GlcNzRdeadi8Yc4130_provenance.