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- source_evidence_literature type ECO_0000212 NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.
- NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_assertion description "[X-linked hypophosphatemic rickets/osteomalacia (XLH), autosomal dominant and recessive hypophosphatemic rickets/osteomalacia (ADHR and ARHR) share common clinical features including high fibroblast growth factor 23 (FGF23) levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.
- NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_assertion evidence source_evidence_literature NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.
- NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_assertion SIO_000772 19581284 NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.
- NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_assertion wasDerivedFrom befree-2016 NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.
- NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_assertion wasGeneratedBy ECO_0000203 NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.
- befree-2016 importedOn "2016-02-19" NP749511.RASa2GapVW2GTbFKF_8VER2jDX-Z0Y0cAenD3x0IMA-XU130_provenance.