Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.
- NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_assertion description "[Recent cytogenetic and molecular analyses have shown that most LGFMSs have a characteristic chromosomal abnormality, t(7;16)(q33;p11), resulting in the FUS-CREB3L2 fusion gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.
- NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_assertion evidence source_evidence_literature NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.
- NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_assertion SIO_000772 16931951 NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.
- NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_assertion wasDerivedFrom befree-20140225 NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.
- NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_assertion wasGeneratedBy ECO_0000203 NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP450932.RA2Hiy1zuvEqJBnciIZhGojSfShaReOm6eBpfOa4lBb2Y130_provenance.