Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.
- NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_assertion description "[One candidate gene in the region, MYH7, which is mutated in cardiomyopathy and myosin storage myopathy, codes for the myosin heavy chain of type I skeletal muscle fibers and cardiac ventricles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.
- NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_assertion evidence source_evidence_literature NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.
- NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_assertion SIO_000772 15322983 NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.
- NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_assertion wasDerivedFrom befree-20140225 NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.
- NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_assertion wasGeneratedBy ECO_0000203 NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914707.RAAKyLhaky5v5rPng3p6IK6p6CjLCHR274Nv77Ipfom6c130_provenance.