Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.
- NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_assertion wasGeneratedBy ECO_0000203 NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.
- NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_assertion wasDerivedFrom befree-20150227 NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.
- NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_assertion SIO_000772 20522425 NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.
- NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_assertion evidence source_evidence_literature NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.
- NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_assertion description "[Methods In this context, a search was undertaken for mutations in LMNA, encoding Lamins A/C, and ZMPSTE24, LBR, LMNB1, LMNB2, MAN1, SYNE1a and LAP2, encoding Lamins A/C molecular partners, in a Caucasian woman affected with Reynolds syndrome, a particular nosologic entity specifically associating limited cutaneous SSc and primary biliary cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742772.RAUPFZvLyoznvbeSgV_0nR9i9zcH-LNKy7B0FIbwOiMGo130_provenance.