Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_assertion> ?p ?o ?g. }
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- NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_assertion type Assertion NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_head.
- NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_assertion description "[Germline mutations in the LKB1/STK11 tumour suppressor gene cause Peutz-Jeghers syndrome (PJS), a rare dominant disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_provenance.
- NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_assertion evidence source_evidence_literature NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_provenance.
- NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_assertion SIO_000772 12865922 NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_provenance.
- NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_assertion wasDerivedFrom befree-20150227 NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_provenance.
- NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_assertion wasGeneratedBy ECO_0000203 NP759137.RAVBHMGc1jEoUup0ngrf_tn_1Y49jlDA59mCftG-wwwCQ130_provenance.