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- source_evidence_literature type ECO_0000212 NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.
- NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_assertion description "[In 5 patients with MEN 2A, gene rearrangements, such as a gross deletion, were not found in the 880 kb NruI fragment which covered the closest region to the MEN-2A locus from the RBP3 and D10S15 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.
- NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_assertion evidence source_evidence_literature NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.
- NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_assertion SIO_000772 1982737 NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.
- NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_assertion wasDerivedFrom befree-20150227 NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.
- NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_assertion wasGeneratedBy ECO_0000203 NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP363138.RAHCV2C7xmx_zlqjmdPVX3JxrM1-1_A0d-bFE45bYZs2M130_provenance.