Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_assertion type Assertion NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_head.
- NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_assertion description "[We describe the phenotypic characteristics associated with interstitial deletion of the p14-16 region of chromosome 4 in 7 patients with multiple minor anomalies in common, and with mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_provenance.
- NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_assertion evidence source_evidence_literature NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_provenance.
- NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_assertion SIO_000772 7573135 NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_provenance.
- NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_assertion wasDerivedFrom befree-20140225 NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_provenance.
- NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_assertion wasGeneratedBy ECO_0000203 NP663941.RABL_5hWiNxKHBkDshroElSq1h3Wd94vwNH604oxY8H1g130_provenance.