Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_assertion> ?p ?o ?g. }
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- NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_assertion type Assertion NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_head.
- NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_assertion description "[Heterozygous germline mutations of the tumor-suppressor gene MEN1 are responsible for multiple endocrine neoplasia type 1 (MEN1), a dominantly inherited familial cancer syndrome characterized by pituitary, parathyroid, and enteropancreatic tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_provenance.
- NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_assertion evidence source_evidence_literature NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_provenance.
- NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_assertion SIO_000772 19068082 NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_provenance.
- NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_assertion wasDerivedFrom befree-2016 NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_provenance.
- NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_assertion wasGeneratedBy ECO_0000203 NP708155.RA69TvAq1u8jIlZ0KHyk2y6JllN7ozFB_s0iXRroTxEBQ130_provenance.