Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.
- NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_assertion wasGeneratedBy ECO_0000203 NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.
- NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_assertion wasDerivedFrom befree-20150227 NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.
- NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_assertion SIO_000772 18371931 NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.
- NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_assertion evidence source_evidence_literature NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.
- NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_assertion description "[We demonstrate that the pcy mutation generates a hypomorphic Nphp3 allele that is responsible for the cystic kidney disease phenotype, whereas complete loss of Nphp3 function results in situs inversus, congenital heart defects, and embryonic lethality in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884684.RATnmGRSxQtmb4Ufb11hrwP5ObXVjp0pQD0mggrpfur9E130_provenance.