Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.
- NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_assertion wasGeneratedBy ECO_0000203 NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.
- NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_assertion wasDerivedFrom befree-20150227 NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.
- NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_assertion SIO_000772 22971997 NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.
- NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_assertion evidence source_evidence_literature NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.
- NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_assertion description "[The autosomal dominant form of FSGS is a heterogenic disease caused by mutations within three known genes: α-actinin 4 (ACTN4), canonical transient receptor potential 6 (TRPC6), and the inverted formin 2 (INF2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222027.RAcJBtZP1wtbJcxM3hi6AJuFYs_K6mZmBYV7JL0lI4gjI130_provenance.