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- source_evidence_literature type ECO_0000212 NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.
- NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_assertion description "[Because 1) HGF and c-met map to chromosome 7q21 and 7q31, respectively, 2) FTC loses genetic material at multiple loci with a frequency much higher than PTC, and 3) loss of heterozygosity (LOH) on 7q has been previously found in various tumors, we tested the hypothesis that both FTC and ATC, but not PTC, could harbor LOH in segments of 7q encompassing the loci for HGF and c-met.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.
- NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_assertion evidence source_evidence_literature NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.
- NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_assertion SIO_000772 10487693 NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.
- NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_assertion wasDerivedFrom befree-20150227 NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.
- NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_assertion wasGeneratedBy ECO_0000203 NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP498545.RAwhUioXoA9cp3PRuXy8IAG-wweJZ5ZKU_6zMrZwA5LhA130_provenance.