Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.
- NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_assertion wasGeneratedBy ECO_0000203 NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.
- NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_assertion wasDerivedFrom befree-20150227 NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.
- NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_assertion SIO_000772 17216245 NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.
- NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_assertion evidence source_evidence_literature NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.
- NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_assertion description "[The DNA sequence analysis of the polymerase chain reaction (PCR) detected no mutations in the NPHP2 (INVS) gene in this child, suggesting that new mutant genes might be responsible for the early onset of ESRD in infantile NPHP with features of JBTS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886229.RAx4dRXCJjJQSPaeVFM2-GbnQV0Qu1ZDVWjMND5LkjGyc130_provenance.