Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_assertion> ?p ?o ?g. }
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- NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_assertion type Assertion NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_head.
- NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_assertion description "[This rare disease is associated with loss of heterozygosity (LOH) on chromosome 11q13, the locus of the MEN-1 gene, although the MEN-1 sequence and expression appear normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_provenance.
- NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_assertion evidence source_evidence_literature NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_provenance.
- NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_assertion SIO_000772 10690880 NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_provenance.
- NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_assertion wasDerivedFrom befree-20140225 NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_provenance.
- NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_assertion wasGeneratedBy ECO_0000203 NP162160.RAgd2Yb0C-bzhIuD6Fl1lUzz4q_yPx0eB9qrMHr_AJGPo130_provenance.