Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- befree-2016 importedOn "2016-02-19" NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion wasGeneratedBy ECO_0000203 NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion wasDerivedFrom befree-2016 NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion SIO_000772 1481806 NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion evidence source_evidence_literature NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_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." NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.