Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.
- NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_assertion description "[The basic molecular work-up included analysis of concordance based on 10 polymorphic markers (D3S1358, vVA, FGA, amelogenin, D8S1179, D21S11, D18S51, D5S818, D13S317, D7S820) and exclusion of the major slit-diaphragm gene mutation (NPHS2, CD2AP, WT1) causing nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.
- NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_assertion evidence source_evidence_literature NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.
- NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_assertion SIO_000772 16382323 NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.
- NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_assertion wasDerivedFrom befree-2016 NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.
- NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_assertion wasGeneratedBy ECO_0000203 NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.
- befree-2016 importedOn "2016-02-19" NP528763.RAjeLMqv80Fa7dqa5uA40A8OORdrNcjO_uabeXbnfsFzs130_provenance.