Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.
- NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_assertion description "[Inactivating mutations of CDKN1B, encoding the p27 cyclin-dependent kinase inhibitor, were reported to cause hyperparathyroidism in a multiple endocrine neoplasia type 1-like syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.
- NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_assertion evidence source_evidence_literature NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.
- NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_assertion SIO_000772 18288099 NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.
- NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_assertion wasDerivedFrom befree-2016 NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.
- NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_assertion wasGeneratedBy ECO_0000203 NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.
- befree-2016 importedOn "2016-02-19" NP656504.RAYVKRlEvv-O9aOqB8kYD98voC9afEa26Dq0Lt19Muclk130_provenance.