Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.
- NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_assertion wasGeneratedBy ECO_0000203 NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.
- NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_assertion wasDerivedFrom befree-20140225 NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.
- NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_assertion SIO_000772 21683322 NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.
- NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_assertion evidence source_evidence_literature NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.
- NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_assertion description "[After exome sequencing in GD and AD cases, we selected fibrillin 1 (FBN1) as a candidate gene, even though mutations in this gene have been described in Marfan syndrome, which is characterized by tall stature and arachnodactyly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP849059.RAl-bMPFiWIC2PFzuTtYAJ7a_8tuoelKHF5jG2HHWWl8Q130_provenance.