Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.
- NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_assertion description "[X-linked hypophosphatemia (XLH) is phenotypically similar to OHO and results from mutations in PHEX, a putative metallopeptidase believed to process a factor(s) regulating bone mineralization and renal phosphate reabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.
- NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_assertion evidence source_evidence_literature NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.
- NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_assertion SIO_000772 11414762 NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.
- NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_assertion wasDerivedFrom befree-2016 NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.
- NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_assertion wasGeneratedBy ECO_0000203 NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.
- befree-2016 importedOn "2016-02-19" NP321434.RAO9Zpx8KaOGV8KFyAPHXwShd18MzJhEKkRl45CUdzZ0M130_provenance.