Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP897107.RAD_g67b0ltXCxRJmcHEbtqiJNSuHyt1oQjiGdh75wAtw130_provenance.