Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion> ?p ?o ?g. }
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- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion type Assertion NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_head.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion description "[One novel deletion and one splicing mutation of the LKB1 gene in two Chinese patients with Peutz-Jeghers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion evidence source_evidence_literature NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion SIO_000772 22928647 NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion wasDerivedFrom befree-2016 NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion wasGeneratedBy ECO_0000203 NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.