Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.
- NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_assertion description "[Three congenital disorders have been localised to this region: blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), Charcot-Marie-Tooth neuropathy type IIB (CMT2B) and Mobius syndrome type 2 (MBS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.
- NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_assertion evidence source_evidence_literature NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.
- NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_assertion SIO_000772 10830911 NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.
- NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_assertion wasDerivedFrom befree-20150227 NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.
- NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_assertion wasGeneratedBy ECO_0000203 NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP785713.RABF8TR5BwdUoN4Sbml15p7tLf8oaX6fifzBjJFMp5GqI130_provenance.