Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.
- NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_assertion description "[Germline mutations in the LKB1/STK11 tumour suppressor gene cause Peutz-Jeghers syndrome (PJS), a rare dominant disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.
- NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_assertion evidence source_evidence_literature NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.
- NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_assertion SIO_000772 12865922 NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.
- NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_assertion wasDerivedFrom befree-2016 NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.
- NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_assertion wasGeneratedBy ECO_0000203 NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.
- befree-2016 importedOn "2016-02-19" NP402106.RAJ8o9VOKxW9fgeUGGfoP5SJGwtvDfjan-YH3NYHgR7Go130_provenance.