Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_assertion> ?p ?o ?g. }
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- NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_assertion type Assertion NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_head.
- NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_assertion wasGeneratedBy ECO_0000203 NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_provenance.
- NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_assertion wasDerivedFrom befree-20140225 NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_provenance.
- NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_assertion SIO_000772 9384616 NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_provenance.
- NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_assertion evidence source_evidence_literature NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_provenance.
- NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_assertion description "[As liver Phk deficiency is generally a benign condition and progression to cirrhosis is very rare, this finding suggests that PHKG2 mutations are associated with an increased cirrhosis risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363398.RAPCxfjYInImhZH0ItynDhACiKLpXLDa_zTG214pHMAT4130_provenance.