Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.
- NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_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." NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.
- NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_assertion evidence source_evidence_literature NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.
- NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_assertion SIO_000772 10830911 NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.
- NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_assertion wasDerivedFrom befree-20140225 NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.
- NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_assertion wasGeneratedBy ECO_0000203 NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP644021.RAunMu4NuDLolkqAqPLH-4f2Bw0GtVPsVrS7gM592FiYw130_provenance.