Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_assertion> ?p ?o ?g. }
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- NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_assertion type Assertion NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_head.
- NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_assertion wasGeneratedBy ECO_0000203 NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_provenance.
- NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_assertion wasDerivedFrom befree-20140225 NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_provenance.
- NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_assertion SIO_000772 14694057 NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_provenance.
- NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_assertion evidence source_evidence_literature NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_provenance.
- NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_assertion description "[The authors report on a patient homozygous for a recessive missense mutation in POLG who presented with a multisystem disorder without PEO.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795688.RAA4gNahfoykJDHyWjvh4nlCvrPFihFTq9Rq0TRwK5084130_provenance.