Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.
- NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_assertion wasGeneratedBy ECO_0000203 NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.
- NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_assertion wasDerivedFrom befree-20150227 NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.
- NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_assertion SIO_000772 23335257 NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.
- NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_assertion evidence source_evidence_literature NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.
- NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_assertion description "[Segmental copy number loss in the region of Semaphorin 4D gene in patients with acetabular dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845038.RAwK2RVssS4RFrl8HOKc3n0F5xzsj-dXrdlGK0LlAFCFw130_provenance.