Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.
- NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_assertion description "[ The results demonstrate that NPHS2 mutations are also present in Chinese sporadic SRNS. Our investigation supports the necessity of searching for mutations in NPHS2 in Chinese children with sporadic SRNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.
- NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_assertion evidence source_evidence_literature NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.
- NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_assertion SIO_000772 15769810 NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.
- NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_assertion wasDerivedFrom gad-20150221 NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.
- NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_assertion wasGeneratedBy ECO_0000203 NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67407.RAoGH-PqOPDlc6N1-26rb6_RGYCZ-ApaYqpJOcK2IvlbY130_provenance.