Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_assertion> ?p ?o ?g. }
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- NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_assertion type Assertion NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_head.
- NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_assertion description "[The exclusion of the EVC region in ATD and SRP III families suggests that locus heterogeneity exists within the short-rib dysplasia (with and without polydactyly) group of disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_provenance.
- NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_assertion evidence source_evidence_literature NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_provenance.
- NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_assertion SIO_000772 10951528 NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_provenance.
- NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_assertion wasDerivedFrom befree-20140225 NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_provenance.
- NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_assertion wasGeneratedBy ECO_0000203 NP693905.RACgFEDtxb2O9K-OhT3ohQnwKIL1r5M8_F0ABoDosBzGA130_provenance.