Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.
- NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_assertion description "[Germline mutations in MEN1 (encoding menin) result in multiple endocrine neoplasia type 1 and are found in very young patients with isolated sporadic pituitary adenomas, which highlights the importance of the chromosome 11q13 locus in pituitary tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.
- NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_assertion evidence source_evidence_literature NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.
- NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_assertion SIO_000772 25350067 NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.
- NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_assertion wasDerivedFrom befree-2016 NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.
- NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_assertion wasGeneratedBy ECO_0000203 NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1233107.RA6ScHNDIh8AVpZYlAI13RLA68u3wGWkOecdYtxK487zc130_provenance.