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- source_evidence_literature type ECO_0000212 NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.
- NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_assertion description "[Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.
- NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_assertion evidence source_evidence_literature NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.
- NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_assertion SIO_000772 10982477 NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.
- NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_assertion wasDerivedFrom befree-2016 NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.
- NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_assertion wasGeneratedBy ECO_0000203 NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.
- befree-2016 importedOn "2016-02-19" NP294790.RA2cglK0_Get7trWmyEkrbXu2qh-uB2K_7-wiHFbGI65g130_provenance.