Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_assertion> ?p ?o ?g. }
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- NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_assertion type Assertion NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_head.
- NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_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." NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_provenance.
- NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_assertion evidence source_evidence_literature NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_provenance.
- NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_assertion SIO_000772 12865922 NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_provenance.
- NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_assertion wasDerivedFrom befree-20140225 NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_provenance.
- NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_assertion wasGeneratedBy ECO_0000203 NP257516.RAVhNm_PtnuPxiqfIYUYF-87ycjqZq4dawjbPe14q-JLE130_provenance.