Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.
- NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_assertion description "[Recently, mutations in Latent Transforming Growth Factor (TGF)-beta Binding Protein 2 (LTBP2) have been reported in several families that were diagnosed with PCG, who actually had a more complex ocular phenotype with ectopia lentis and Marfanoid features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.
- NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_assertion evidence source_evidence_literature NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.
- NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_assertion SIO_000772 22924778 NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.
- NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_assertion wasDerivedFrom befree-2016 NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.
- NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_assertion wasGeneratedBy ECO_0000203 NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1008295.RAfKLuQPx2O95J8Qplci2goDO0PCCrD7pesXo8rASnxkI130_provenance.