Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.
- NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_assertion description "[Familial isolated primary hyperparathyroidism (FIHP) is an autosomal dominant disorder that can represent an early stage of either the multiple endocrine neoplasia type 1 (MEN1) or hyperparathyroidism-jaw tumor (HPT-JT) syndromes; alternatively, the condition can be caused by an allelic variant of MEN1 or HRPT2 (hyperparathyroidism 2 gene), or caused by a distinct entity involving another locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.
- NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_assertion evidence source_evidence_literature NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.
- NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_assertion SIO_000772 18084346 NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.
- NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_assertion wasDerivedFrom befree-2016 NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.
- NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_assertion wasGeneratedBy ECO_0000203 NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.
- befree-2016 importedOn "2016-02-19" NP645570.RApTXMxvtOxJ8qd5lkf66QIIriE5cFSbxHl3RFSx9KDGM130_provenance.