Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.
- NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_assertion description "[Although the most studied clinical syndrome with CDP, rhizomelic chondrodysplasia punctata (RCDP), is known to be caused by several different abnormalities of plasmalogen biosynthesis, there are many other genetic disorders with CDP for which the biochemical cause is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.
- NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_assertion evidence source_evidence_literature NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.
- NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_assertion SIO_000772 10096601 NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.
- NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_assertion wasDerivedFrom befree-20140225 NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.
- NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_assertion wasGeneratedBy ECO_0000203 NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP534025.RAF23P6OlCV843kGpK5jUrFYMn1hYXJAO96gR1ZQk9J8E130_provenance.