Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.
- NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_assertion description "[This study implicates nine different loci involved in genetic susceptibility to Dupuytrens disease. The fact that six of these nine loci harbor genes encoding proteins in the Wnt-signaling pathway suggests that aberrations in this pathway are key to the process of fibromatosis in Dupuytrens disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.
- NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_assertion evidence source_evidence_literature NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.
- NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_assertion SIO_000772 21732829 NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.
- NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_assertion wasDerivedFrom gad-20130706 NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.
- NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_assertion wasGeneratedBy ECO_0000203 NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.
- gad-20130706 importedOn "2013-07-06" NP96238.RALXfxPibxzFiL_JT8vrNIZOSsRcxLuvhJM1ZT5AzUJe8130_provenance.