Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion type Assertion NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_head.
- NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion wasGeneratedBy ECO_0000203 NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_provenance.
- NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion wasDerivedFrom befree-20140225 NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_provenance.
- NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion SIO_000772 19785597 NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_provenance.
- NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion evidence source_evidence_literature NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_provenance.
- NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion description "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_provenance.