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- source_evidence_literature type ECO_0000212 NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.
- NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_assertion description "[We analyzed 6 MTCs and 1 C-cell hyperplasia (CCH) specimen from 7 patients with MEN2A and RET germline mutations in codons 609, 618, 620, or 634, using microdissection, microsatellite analysis, phosphorimage densitometry, and VHL mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.
- NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_assertion evidence source_evidence_literature NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.
- NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_assertion SIO_000772 16707008 NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.
- NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_assertion wasDerivedFrom befree-20140225 NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.
- NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_assertion wasGeneratedBy ECO_0000203 NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP794398.RA1MoYieWhgbS50ucMUxEuWmMlOyPKY3uEkjfELtyj5gI130_provenance.