Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_assertion> ?p ?o ?g. }
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- NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_assertion type Assertion NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_head.
- NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_assertion description "[Hemihypertrophy was strongly associated with UPD (P<0.0001) and exomphalos was associated with an IC2 defect or CDKN1C mutation but not UPD or IC1 defect (P<0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.
- NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_assertion evidence source_evidence_literature NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.
- NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_assertion SIO_000772 15999116 NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.
- NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_assertion wasDerivedFrom befree-20140225 NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.
- NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_assertion wasGeneratedBy ECO_0000203 NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.