Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion type Assertion NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_head.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_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." NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion evidence source_evidence_literature NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion SIO_000772 17665217 NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion wasDerivedFrom befree-20140225 NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion wasGeneratedBy ECO_0000203 NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.