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- source_evidence_literature type ECO_0000212 NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.
- NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_assertion description "[The genetic variants associated with the risk of glioma in the EGFR gene have also been associated with specific somatic aberrations, including loss at the CDKN2A/B locus and allele specific loss of EGFR in the tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.
- NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_assertion evidence source_evidence_literature NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.
- NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_assertion SIO_000772 24184969 NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.
- NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_assertion wasDerivedFrom befree-2016 NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.
- NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_assertion wasGeneratedBy ECO_0000203 NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1124454.RAUZgmv9JmuhNhBfKTseNUL-19xhztd4tUWHBQbyPQXfs130_provenance.