Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.
- NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_assertion description "[Genetic analysis revealed that 1) PEO1 has a major role in determining familial PEO, since it accounts for 26.8% of familial cases, followed by ANT1 (14.6%) and POLG1 (9.8%); 2) no mutations in any of the known genes were found in 53.7% of probands of this series.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.
- NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_assertion evidence source_evidence_literature NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.
- NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_assertion SIO_000772 18575922 NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.
- NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_assertion wasDerivedFrom gad-20150221 NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.
- NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_assertion wasGeneratedBy ECO_0000203 NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP124528.RAcE6CmJxw6KW5xsU1c6NRw5LzEDeMujJOacOK1PVCUJE130_provenance.