Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.
- NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion description "[These findings indicate that approximately half of the variance in mean s.c. abd. AS can be attributed to familial factors and that genetic variation in LMNA might not only underlie rare cases of FPLD, but may also contribute to variation in adipocyte size in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.
- NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion evidence source_evidence_literature NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.
- NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion SIO_000772 11243729 NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.
- NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion wasDerivedFrom gad-20130706 NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.
- NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion wasGeneratedBy ECO_0000203 NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance.