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- source_evidence_literature type ECO_0000212 NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.
- NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_assertion description "[In a nationwide study conducted in Japan between 1999 and 2009, the authors identified 51 different L1CAM gene mutations in 56 families with XLH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.
- NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_assertion evidence source_evidence_literature NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.
- NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_assertion SIO_000772 21961551 NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.
- NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_assertion wasDerivedFrom befree-20150227 NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.
- NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_assertion wasGeneratedBy ECO_0000203 NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768661.RAK5dRUct0Qugr_Jbz6yir8Eu1YOb7VhdWrm-pXCZn0Fc130_provenance.