Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.
- NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_assertion description "[The phenotypic expression of partial lipodystrophy is present in two familial syndromes: familial partial lipodystrophy type 1 (FPLD1), with fat loss from the extremities, and central obesity and FPLD type 2, with fat loss from the extremities, abdomen, and thorax.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.
- NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_assertion evidence source_evidence_literature NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.
- NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_assertion SIO_000772 12766116 NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.
- NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_assertion wasDerivedFrom befree-2016 NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.
- NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_assertion wasGeneratedBy ECO_0000203 NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.
- befree-2016 importedOn "2016-02-19" NP395519.RARGtDOy5T7sXi8FD0RN-d3CjjRurWEbW1ohpsqcpU_oA130_provenance.