Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.
- NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_assertion wasGeneratedBy ECO_0000203 NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.
- NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_assertion wasDerivedFrom befree-20140225 NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.
- NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_assertion SIO_000772 20522425 NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.
- NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_assertion evidence source_evidence_literature NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.
- NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_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." NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP885636.RAOjWzC-ancR2s42_2D0Gp1BZi9KY50aL2EtemMn3AV_g130_provenance.