Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.
- NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_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." NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.
- NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_assertion evidence source_evidence_literature NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.
- NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_assertion SIO_000772 16382323 NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.
- NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_assertion wasDerivedFrom befree-20140225 NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.
- NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_assertion wasGeneratedBy ECO_0000203 NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP448906.RA3V5Mqhgu8dnwPw74D2p87ge6ZwXJYAdogayV6LBmesg130_provenance.