Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.
- NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_assertion description "[The aim of this work was to screen mutations and polymorphisms of the TRPC6 gene in a group of 64 Czech patients with nephrotic syndrome and subsequently, on the basis of these data, evaluate the role of mutations in the TRPC6 gene in Czech population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.
- NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_assertion evidence source_evidence_literature NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.
- NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_assertion SIO_000772 22980509 NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.
- NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_assertion wasDerivedFrom befree-2016 NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.
- NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_assertion wasGeneratedBy ECO_0000203 NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1013001.RACH7W4_HwPmeGsCzZY49VbjBIoFCAxDNGwmSZq2U1EGI130_provenance.