Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_assertion> ?p ?o ?g. }
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- NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_assertion type Assertion NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_head.
- NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_assertion description "[In the present study, we have identified a large number of mutations in SLC17A5 in patients presenting with either Salla disease or the ISSD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_provenance.
- NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_assertion evidence source_evidence_curated NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_provenance.
- NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_assertion SIO_000772 10947946 NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_provenance.
- NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_assertion wasDerivedFrom uniprot-2016 NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_provenance.
- NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_assertion wasGeneratedBy ECO_0000218 NP971.RAWu6g7jJ9QpZoS8LoEPi706IMy2PNsmSRN2WXQwtMsRw130_provenance.