Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion type Assertion NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_head.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion wasGeneratedBy ECO_0000203 NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion wasDerivedFrom befree-20140225 NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion SIO_000772 19785597 NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion evidence source_evidence_literature NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_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." NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.