Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP273274.RA13HM2Tif31gtU9LOwKNgussCM6Sfwk4_sou76CthmxU130_provenance.