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- source_evidence_literature type ECO_0000212 NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.
- NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_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." NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.
- NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_assertion evidence source_evidence_literature NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.
- NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_assertion SIO_000772 10487693 NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.
- NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_assertion wasDerivedFrom befree-2016 NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.
- NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_assertion wasGeneratedBy ECO_0000203 NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.
- befree-2016 importedOn "2016-02-19" NP263119.RANUuhAFeiS8RHxZCfjkz7PutL72LYq_nq5BgYEL0gbLE130_provenance.