Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.
- NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_assertion wasGeneratedBy ECO_0000203 NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.
- NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_assertion wasDerivedFrom befree-20150227 NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.
- NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_assertion SIO_000772 11595624 NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.
- NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_assertion evidence source_evidence_literature NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.
- NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_assertion description "[The cell line did express PHEX (phosphate-regulating gene with homologies to endopeptidases located on the X-chromosome) and FGF-23 (fibroblast growth factor-23) transcripts on northern hybridization; however, none of the known mutations from the related mendelian disorders of X-linked hypophosphatemic rickets or autosomal-dominant hypophosphatemic rickets could be detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789583.RAHwXr3FyjAr3b6W3GU-Rn5YiWCbh9nNU5dF0QxjjmVdg130_provenance.