Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_assertion type Assertion NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_head.
- NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_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." NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_provenance.
- NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_assertion evidence source_evidence_literature NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_provenance.
- NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_assertion SIO_000772 19068082 NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_provenance.
- NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_assertion wasDerivedFrom befree-2016 NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_provenance.
- NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_assertion wasGeneratedBy ECO_0000203 NP708154.RABPnIfunCoB1vRn5LdX0crOHhhZsptOi5c28nUK5HzZk130_provenance.