Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_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." NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_assertion evidence source_evidence_literature NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_assertion SIO_000772 11854170 NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_assertion wasDerivedFrom befree-20140225 NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_assertion wasGeneratedBy ECO_0000203 NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP340121.RAamZiWebedU943-vLgi4rLr1Ov5njUNkV18Ai6HemJ9M130_provenance.