Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_assertion type Assertion NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_head.
- NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_assertion description "[Multiple osteochondromas (MO) is an autosomal dominant hereditary disorder caused by heterozygous germline mutations in the exostonsin-1 (EXT1) or exostosin-2 (EXT2) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_provenance.
- NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_assertion evidence source_evidence_literature NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_provenance.
- NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_assertion SIO_000772 23629877 NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_provenance.
- NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_assertion wasDerivedFrom befree-2016 NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_provenance.
- NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_assertion wasGeneratedBy ECO_0000203 NP1073514.RAP1DigOv1SboBi10dfPlc7ysxBLCimlJiUp99Gt_neHY130_provenance.