Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.
- NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_assertion description "[PROP1 gene mutations lead to combined pituitary deficiency, and HESX gene mutations result in septo-optic dysplasia, both of which include HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.
- NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_assertion evidence source_evidence_literature NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.
- NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_assertion SIO_000772 10727999 NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.
- NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_assertion wasDerivedFrom befree-20140225 NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.
- NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_assertion wasGeneratedBy ECO_0000203 NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP675358.RAfzocprcKKDNUXL5byCXHSLlwpIUm47VtGp8atRqVbo0130_provenance.