Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.
- NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_assertion description "[Patterns of X-chromosome inactivation were determined by means of polymerase chain reaction amplification of the CAG-nucleotide repeat of the androgen receptor (AR) gene after methylation-sensitive restriction endonuclease digestion of blood mononuclear cell DNA from patients with invasive (n = 213) or borderline (n = 44) ovarian cancer and control subjects without a personal or family history of cancer (n = 50).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.
- NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_assertion evidence source_evidence_literature NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.
- NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_assertion SIO_000772 10050867 NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.
- NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_assertion wasDerivedFrom befree-20140225 NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.
- NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_assertion wasGeneratedBy ECO_0000203 NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP215953.RAmE3F0Xif9K2oRnXRW7_hHQjax3PVyUlWQOZPn4yIFZo130_provenance.