Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_assertion> ?p ?o ?g. }
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- NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_assertion type Assertion NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_head.
- NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_assertion wasGeneratedBy ECO_0000203 NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_provenance.
- NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_assertion wasDerivedFrom befree-2016 NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_provenance.
- NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_assertion SIO_000772 16724007 NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_provenance.
- NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_assertion evidence source_evidence_literature NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_provenance.
- NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_assertion description "[Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551491.RALis4mSou9wLGQXwhafLZcGNu9hugoEfFVNYCycBmiSg130_provenance.