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- source_evidence_literature type ECO_0000212 NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
- NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_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." NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
- NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_assertion evidence source_evidence_literature NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
- NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_assertion SIO_000772 19854292 NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
- NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_assertion wasDerivedFrom befree-20150227 NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
- NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_assertion wasGeneratedBy ECO_0000203 NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP953423.RAnF22Z4N7BJMybQPEwfx-BzbivH4L6qPW8BkH3Zp0Ra4130_provenance.