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- source_evidence_literature type ECO_0000212 NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.
- NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_assertion description "[Mutation analysis was carried out by direct sequencing of the NPHS1 and NPHS2 genes in 145 nephrotic syndrome (NS) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.
- NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_assertion evidence source_evidence_literature NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.
- NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_assertion SIO_000772 22565185 NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.
- NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_assertion wasDerivedFrom befree-2016 NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.
- NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_assertion wasGeneratedBy ECO_0000203 NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.
- befree-2016 importedOn "2016-02-19" NP980278.RAwJub7JDXgxbJCoHM1J4OC6H_QkJjxI_DZAWKHX74Mrs130_provenance.