Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.
- NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_assertion description "[Using microsatellite analysis, Southern blot analysis, and fluorescence in situ hybridization (FISH), 30 primary tumors and six CSF metastasis specimens were analyzed for loss of heterozygosity (LOH) of chromosomes 1q31, 6q, 9q22, 10q, 11, 16q22, and 17p13.1 and/or high-level amplification of the c-myc gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.
- NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_assertion evidence source_evidence_literature NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.
- NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_assertion SIO_000772 9667267 NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.
- NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_assertion wasDerivedFrom befree-20140225 NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.
- NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_assertion wasGeneratedBy ECO_0000203 NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP328383.RAhkeVL4YWyjpWDiEbjxRruC13l0U1_C2nikhKEQ2n72g130_provenance.