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- source_evidence_literature type ECO_0000212 NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.
- NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_assertion description "[The clinical and genetic aspects of these families confirm that this syndrome can be clinically variable, with different mutations in the FGFR2 responsible for PS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.
- NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_assertion evidence source_evidence_literature NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.
- NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_assertion SIO_000772 25129254 NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.
- NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_assertion wasDerivedFrom befree-2016 NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.
- NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_assertion wasGeneratedBy ECO_0000203 NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1211267.RASBLUsqGzimo10-_ayFpPGmvJV2xVO7NKJ9mPfovf5Xk130_provenance.