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- source_evidence_literature type ECO_0000212 NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.
- NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_assertion description "[Additionally, a patient with the severe, autosomal recessive, infantile form of osteopetrosis (ARO) was identified as being homozygous for a ClCN7 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.
- NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_assertion evidence source_evidence_literature NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.
- NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_assertion SIO_000772 11741829 NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.
- NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_assertion wasDerivedFrom befree-2016 NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.
- NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_assertion wasGeneratedBy ECO_0000203 NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.
- befree-2016 importedOn "2016-02-19" NP338745.RAxXK_KN8wfek1_M_sajansH4ldina3qsD0l8YulKUeXc130_provenance.