Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.
- NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_assertion description "[Our results therefore support the exclusion of ATP2B3 as the causal disease gene of XLMTM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.
- NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_assertion evidence source_evidence_literature NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.
- NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_assertion SIO_000772 8931700 NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.
- NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_assertion wasDerivedFrom befree-20150227 NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.
- NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_assertion wasGeneratedBy ECO_0000203 NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256563.RAS9RCD4Ot_6zxUVI8EqjRGiP6qyIqGC9WuSEY4TOVuKc130_provenance.