Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_assertion type Assertion NP799711.RAwhTZGklK0cR3J1gIdC4EVtqR2jbgDj-zL3q06L4ZzUI130_head.
- 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.