Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_assertion> ?p ?o ?g. }
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- NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_assertion type Assertion NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_head.
- NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_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." NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_provenance.
- NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_assertion evidence source_evidence_literature NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_provenance.
- NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_assertion SIO_000772 19854292 NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_provenance.
- NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_assertion wasDerivedFrom befree-2016 NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_provenance.
- NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_assertion wasGeneratedBy ECO_0000203 NP771463.RAij0mU3SZkTu8-Qut2kfwTeGy_vhR4xphf7zC2UNrJXc130_provenance.