Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.
- NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_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." NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.
- NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_assertion evidence source_evidence_literature NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.
- NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_assertion SIO_000772 10487693 NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.
- NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_assertion wasDerivedFrom befree-20150227 NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.
- NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_assertion wasGeneratedBy ECO_0000203 NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.
- befree-20150227 importedOn "2015-02-27" NP448043.RAjhD8U2UJuVCqb-ig_hWhjT_SFRm0mAqa91Gm-jsRyag130_provenance.