Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_assertion type Assertion NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_head.
- NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_assertion description "[Subsequent fluorescence in-situ hybridization and Array-CGH analyses revealed an unbalanced translocation between 9p and 15q resulting in a partial monosomy of 9p and a partial trisomy of 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.
- NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_assertion evidence source_evidence_literature NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.
- NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_assertion SIO_000772 20671549 NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.
- NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_assertion wasDerivedFrom befree-20140225 NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.
- NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_assertion wasGeneratedBy ECO_0000203 NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.