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- source_evidence_literature type ECO_0000212 NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
- NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
- NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_assertion evidence source_evidence_literature NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
- NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_assertion SIO_000772 19854292 NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
- NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_assertion wasDerivedFrom befree-20140225 NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
- NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_assertion wasGeneratedBy ECO_0000203 NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_provenance.