Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_assertion wasGeneratedBy ECO_0000203 NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_assertion wasDerivedFrom befree-20150227 NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_assertion SIO_000772 9917751 NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_assertion evidence source_evidence_literature NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.
- NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_assertion description "[Hemihypertrophy is also reported as part of the Beckwith-Wiedemann syndrome which has as its cardinal features omphalocele, macroglossia and gigantism with hypoglycemia, organomegaly, renal anomalies, hemihypertrophy, and embryonal tumors occurring less frequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013270.RA-oFycewmw6l6PhKP4JOo282T_wzYJwSJXTeBJ-zgYrA130_provenance.