Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.
- NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_assertion description "[Translocations involving nucleoporin 98kD (NUP98) on chromosome 11p15 occur at relatively low frequency in acute myeloid leukemia (AML) but can be missed with routine karyotyping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.
- NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_assertion evidence source_evidence_literature NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.
- NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_assertion SIO_000772 21813447 NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.
- NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_assertion wasDerivedFrom befree-20140225 NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.
- NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_assertion wasGeneratedBy ECO_0000203 NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP196437.RABH-XU-hRm5PR-TfdTrNDYIhgiDqHMfIaYEEQa4ffl5w130_provenance.