Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_assertion type Assertion NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_head.
- NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_provenance.
- NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_assertion evidence source_evidence_literature NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_provenance.
- NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_assertion SIO_000772 17665217 NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_provenance.
- NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_assertion wasDerivedFrom befree-20140225 NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_provenance.
- NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_assertion wasGeneratedBy ECO_0000203 NP447802.RA6SuSeDtTmACjlRvpq9IRlyW6QTDQGABbTj6QBQVdv0I130_provenance.