Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.
- NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_assertion description "[To investigate the association of the polymorphism of NPHS1, coding gene of nephrin, with the degree of proteinuria, renal function, and prognosis of IgA nephropathy (IgAN) in patients in north China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.
- NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_assertion evidence source_evidence_literature NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.
- NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_assertion SIO_000772 19671286 NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.
- NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_assertion wasDerivedFrom gad-20130706 NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.
- NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_assertion wasGeneratedBy ECO_0000203 NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.
- gad-20130706 importedOn "2013-07-06" NP68897.RAfnSoCTgNe29Gv3MMCpVaro78V5FJ0T1HxSx3K-_m7Ok130_provenance.