Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.
- NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_assertion description "[Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.
- NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_assertion evidence source_evidence_literature NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.
- NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_assertion SIO_000772 10762296 NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.
- NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_assertion wasDerivedFrom befree-20150227 NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.
- NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_assertion wasGeneratedBy ECO_0000203 NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP778161.RABaRw95jLlA7vrenmmmBycsSQwWvskCRc5rTs0RKN5kA130_provenance.