Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_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." NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_assertion evidence source_evidence_literature NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_assertion SIO_000772 17371932 NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_assertion wasDerivedFrom gad-20130706 NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_assertion wasGeneratedBy ECO_0000203 NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66054.RAkf9o2eCelfBD1Q6dujYcNuIcRBsPHewKiIw1BfqkSMU130_provenance.