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- source_evidence_literature type ECO_0000212 NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.
- NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_assertion description "[Functional analysis of HNPCC-related missense mutations in MSH2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.
- NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_assertion evidence source_evidence_literature NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.
- NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_assertion SIO_000772 18822302 NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.
- NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_assertion wasDerivedFrom befree-2016 NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.
- NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_assertion wasGeneratedBy ECO_0000203 NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.
- befree-2016 importedOn "2016-02-19" NP695333.RACTOw514n9ciwqWnh8znud-Shd_suKru_RlZ1UmUHc14130_provenance.