Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_assertion type Assertion NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_head.
- NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_assertion description "[The association of the rare C4B3 variant with microangiopathy suggests a genetic component of its aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_provenance.
- NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_assertion evidence source_evidence_literature NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_provenance.
- NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_assertion SIO_000772 3926068 NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_provenance.
- NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_assertion wasDerivedFrom befree-2016 NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_provenance.
- NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_assertion wasGeneratedBy ECO_0000203 NP1304167.RA9p0xJnZI9uSIrNMDG_-2Zg_jY7rXoen00t2F0AHODC0130_provenance.