Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.
- befree-2016 importedOn "2016-02-19" NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.
- NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_assertion wasGeneratedBy ECO_0000203 NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.
- NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_assertion wasDerivedFrom befree-2016 NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.
- NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_assertion SIO_000772 10424788 NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.
- NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_assertion evidence source_evidence_literature NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.
- NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_assertion description "[Germline MEN1 gene mutations are responsible for multiple endocrine neoplasia type 1 (MEN1), a dominantly inherited cancer syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258789.RAGHYw0kp7VYUtD5exgTHH0xtJOF0uuhsnxQgsNTcSXo8130_provenance.