Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.
- NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_assertion wasGeneratedBy ECO_0000203 NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.
- NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_assertion wasDerivedFrom befree-20150227 NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.
- NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_assertion SIO_000772 10396361 NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.
- NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_assertion evidence source_evidence_literature NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.
- NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_assertion description "[Familial hyperparathyroidism may occur as familial isolated hyperparathyroidism (FIHP) or as part of an inherited syndrome, in particular multiple endocrine neoplasia types 1 and 2A (MEN1, MEN2A) and hyperparathyroidism-jaw tumour (HPT-JT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670698.RAVe6PernnZrB5rCZGvumY3OUbifzGHvvjtTmFxP7vktc130_provenance.