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- source_evidence_literature type ECO_0000212 NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_assertion description "[Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect: muscle-eye-brain disease (MEB), Walker-Warburg syndrome (WWS), and Fukuyama congenital muscular dystrophy (FCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_assertion evidence source_evidence_literature NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_assertion SIO_000772 11320179 NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_assertion wasDerivedFrom befree-20150227 NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_assertion wasGeneratedBy ECO_0000203 NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831588.RAGFLKw4hrMWYRMmaA1982fH1GnhiIuL6Qfe8bidzaz9U130_provenance.