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- source_evidence_literature type ECO_0000212 NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.
- NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_assertion description "[However, mutations in two nuclear proteins--emerin and lamin A/C--have also been demonstrated to give rise to a muscular dystrophy phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.
- NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_assertion evidence source_evidence_literature NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.
- NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_assertion SIO_000772 14585157 NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.
- NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_assertion wasDerivedFrom befree-2016 NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.
- NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_assertion wasGeneratedBy ECO_0000203 NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.
- befree-2016 importedOn "2016-02-19" NP418675.RAnCOcJBNXlPMJyZuZAe_Z7ylhx_rFcDgJMP87Qp1Y4Tw130_provenance.