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- source_evidence_literature type ECO_0000212 NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.
- NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_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." NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.
- NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_assertion evidence source_evidence_literature NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.
- NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_assertion SIO_000772 10487693 NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.
- NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_assertion wasDerivedFrom befree-20150227 NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.
- NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_assertion wasGeneratedBy ECO_0000203 NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP707581.RA3iXv7Kg6rRABvb_wQeqJUBKesWEl8qXy5imbmHsKnFg130_provenance.