Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_assertion> ?p ?o ?g. }
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- NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_assertion type Assertion NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_head.
- NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_assertion wasGeneratedBy ECO_0000218 NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_provenance.
- NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_assertion wasDerivedFrom uniprot-20130724 NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_provenance.
- NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_assertion SIO_000772 12699448 NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_provenance.
- NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_assertion evidence source_evidence_curated NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_provenance.
- NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_assertion description "[Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4012.RAVnhl5FuC49VS4Hx06C1mUSOfcWL8ZzgWX8UHdEIxu2g130_provenance.