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- source_evidence_literature type ECO_0000212 NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.
- NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_assertion description "[Recently, a deletion mutation disrupting both TSC2 and PKD1 has been described in young children with tuberous sclerosis complex with severe renal cystic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.
- NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_assertion evidence source_evidence_literature NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.
- NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_assertion SIO_000772 11812941 NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.
- NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_assertion wasDerivedFrom befree-2016 NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.
- NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_assertion wasGeneratedBy ECO_0000203 NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.
- befree-2016 importedOn "2016-02-19" NP343361.RAXL0sOu4m_2Af1MjwYbjb5BzhGf4dQIEPKqZLzpPcda8130_provenance.