Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.
- NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_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." NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.
- NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_assertion evidence source_evidence_literature NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.
- NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_assertion SIO_000772 23890478 NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.
- NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_assertion wasDerivedFrom befree-20150227 NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.
- NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_assertion wasGeneratedBy ECO_0000203 NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP222142.RAWGcd-ZPLjd_qrdqlV3INC5Fg6Bp9CBrT67pS_nSc7-w130_provenance.