Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.
- NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_assertion wasGeneratedBy ECO_0000203 NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.
- NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_assertion wasDerivedFrom befree-20150227 NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.
- NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_assertion SIO_000772 1481806 NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.
- NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_assertion evidence source_evidence_literature NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.
- NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_assertion description "[A male patient with a de novo proximal interstitial deletion of the short arm of chromosome 1 (46XY, del(1)(p13p22.3) is described with multiple anomalies and developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836357.RA3lNiavlK4LPZkKNS6v0wBjL0U9ZuQPM6WfpIYrJWDEg130_provenance.