Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.
- NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_assertion description "[A double mutation in AGXT gene in families with primary hyperoxaluria type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.
- NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_assertion evidence source_evidence_literature NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.
- NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_assertion SIO_000772 24012869 NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.
- NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_assertion wasDerivedFrom befree-20150227 NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.
- NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_assertion wasGeneratedBy ECO_0000203 NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP230813.RA9uQbhZYDdLQb3YyPWdpWOHbbkCuZcOWdnYnYwSUDKNg130_provenance.