Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_assertion> ?p ?o ?g. }
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- NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_assertion type Assertion NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_head.
- NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_assertion description "[Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_provenance.
- NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_assertion evidence source_evidence_curated NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_provenance.
- NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_assertion SIO_000772 23793026 NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_provenance.
- NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_assertion wasDerivedFrom ctd_human-2016 NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_provenance.
- NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_assertion wasGeneratedBy ECO_0000218 NP33113.RAnB2cWH3o--SA1HoLVYbfADaYwpccvUoSeX7j2jTRJ9A130_provenance.