Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_assertion type Assertion NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_head.
- NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_assertion description "[It has recently been demonstrated that genetic defects in keratin genes cause a number of different skin disorders, including epidermolysis bullosa simplex (EBS), epidermolytic hyperkeratosis (EH), the EH form of epidermal nevi, epidermolytic and non-epidermolytic forms of palmoplantar keratoderma (EPPK and PPK) and pachyonychia congenita (PC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_provenance.
- NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_assertion evidence source_evidence_literature NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_provenance.
- NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_assertion SIO_000772 9023700 NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_provenance.
- NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_assertion wasDerivedFrom befree-20150227 NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_provenance.
- NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_assertion wasGeneratedBy ECO_0000203 NP526423.RAgIHCJoMK4Qez-rkBaMOoat-NSVCMf6NGV2Q8m8BzjTY130_provenance.