Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.
- NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_assertion description "[DA type 5D (DA5D) is a rare, autosomal-recessive DA previously defined by us and is characterized by congenital contractures of the hands and feet, along with distinctive facial features, including ptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.
- NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_assertion evidence source_evidence_literature NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.
- NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_assertion SIO_000772 23261301 NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.
- NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_assertion wasDerivedFrom befree-2016 NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.
- NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_assertion wasGeneratedBy ECO_0000203 NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1038007.RAT4DPhm0IueAd8NPIjCTL7KbyQY2OIgGfh0g_oGb8V8o130_provenance.