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- source_evidence_literature type ECO_0000212 NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_assertion evidence source_evidence_literature NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_assertion SIO_000772 23793026 NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_assertion wasDerivedFrom befree-20150227 NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_assertion wasGeneratedBy ECO_0000203 NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP857948.RAHVa6235Q0Lz9K_0qIrJUcL4tMDW0CZCoFC_RtM0hBmI130_provenance.