Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.
- NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_assertion description "[Hereditary hypophosphatemic rickets with hypercalciuria is a rare metabolic disorder associated with mutations in SLC34A3, the gene that encodes the renal sodium phosphate cotransporter NaPi-IIc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.
- NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_assertion evidence source_evidence_literature NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.
- NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_assertion SIO_000772 18996815 NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.
- NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_assertion wasDerivedFrom befree-20150227 NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.
- NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_assertion wasGeneratedBy ECO_0000203 NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP973828.RAzyo0uzaO1vrW4BXm-XWly8LdPqOkhrGcoAnvCwHUzWs130_provenance.