Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.
- NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_assertion description "[We have identified compound heterozygous missense mutations in POLG1, encoding the mitochondrial DNA polymerase gamma (Pol gamma), in 7 children with progressive encephalopathy from 5 unrelated families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.
- NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_assertion evidence source_evidence_literature NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.
- NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_assertion SIO_000772 16896309 NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.
- NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_assertion wasDerivedFrom befree-20140225 NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.
- NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_assertion wasGeneratedBy ECO_0000203 NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.
- befree-20140225 importedOn "2014-02-25" NP829923.RAUgUecc2FAm2d8TGEw-hZlirCI_SbLjEjRqRGdMcho74130_provenance.