Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.
- NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_assertion wasGeneratedBy ECO_0000203 NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.
- NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_assertion wasDerivedFrom befree-20140225 NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.
- NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_assertion SIO_000772 17216245 NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.
- NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_assertion evidence source_evidence_literature NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.
- NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_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." NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP274719.RAAlPd1_FAMJzzgkJmC5hlHkjKekjvRec5INv7BlHj1Lo130_provenance.