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- source_evidence_literature type ECO_0000212 NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.
- NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_assertion description "[The CFTR gene mutations or IVS8-5T variant in at least 1 allele was identified with similar frequencies among the AZOO (33%) and CRYPTO (21%) patients; 55% of the AZOO patients with normal spermatogenesis (NS) had mutations in 1 or 2 alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.
- NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_assertion evidence source_evidence_literature NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.
- NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_assertion SIO_000772 16572913 NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.
- NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_assertion wasDerivedFrom befree-2016 NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.
- NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_assertion wasGeneratedBy ECO_0000203 NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.
- befree-2016 importedOn "2016-02-19" NP542633.RA6RNYxp43OU47XM1gE7CPNbnVUQYPr_0ixBHmSG-qHy4130_provenance.