Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.
- NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_assertion description "[Mutations of the novel renal glomerular genes NPHS1 and NPHS2 encoding nephrin and podocin cause two types of severe nephrotic syndrome presenting in early life, Finnish type congenital nephrotic syndrome (CNF) and a form of autosomal recessive familial focal segmental glomerulosclerosis (SRN1), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.
- NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_assertion evidence source_evidence_literature NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.
- NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_assertion SIO_000772 11854170 NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.
- NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_assertion wasDerivedFrom befree-20140225 NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.
- NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_assertion wasGeneratedBy ECO_0000203 NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP540980.RA9lYMypZGaQD8bAItEvVoeQB74cHZOvxptyXfRRmBz1A130_provenance.