Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.
- NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_assertion description "[First, two thirds of nephrotic syndrome manifesting in the first year of life can be explained by mutations in 4 genes only (NPHS1, NPHS2, WT1, or LAMB2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.
- NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_assertion evidence source_evidence_literature NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.
- NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_assertion SIO_000772 17371932 NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.
- NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_assertion wasDerivedFrom gad-20150221 NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.
- NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_assertion wasGeneratedBy ECO_0000203 NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP76193.RAlVqnTURo4plZMzygRdfq2eUIiFP1w0_bGUUVWV575HQ130_provenance.