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- source_evidence_literature type ECO_0000212 NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.
- NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_assertion description "[Structural aspects of the p.P222Q homozygous mutation of HSD3B2 gene in a patient with congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.
- NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_assertion evidence source_evidence_literature NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.
- NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_assertion SIO_000772 21340167 NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.
- NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_assertion wasDerivedFrom befree-2016 NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.
- NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_assertion wasGeneratedBy ECO_0000203 NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.
- befree-2016 importedOn "2016-02-19" NP874180.RA-EskCUgF6ACqBKLUaCpr4CEnZrLb9nrXqW634m_sgss130_provenance.