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- source_evidence_literature type ECO_0000212 NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.
- NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_assertion description "[The SSCP technique showed heterozygous defects in the p53 gene in 8 of 39 (20.5%) melanoma tumors: three point mutations in intron sequences (introns 1 and 2) and exon 10, and three new polymorphisms located in introns 1 and 2 (C to T transition at position 11701 in intron 1; C insertion at position 11818 in intron 2; and C insertion at position 11875 in intron 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.
- NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_assertion evidence source_evidence_literature NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.
- NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_assertion SIO_000772 15960923 NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.
- NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_assertion wasDerivedFrom gad-20150221 NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.
- NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_assertion wasGeneratedBy ECO_0000203 NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.
- gad-20150221 importedOn "2015-02-21" NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.