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- source_evidence_literature type ECO_0000212 NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.
- NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_assertion description "[This study showed that CFH was more likely to be AMD susceptibility gene at Chr.1q31 based on the finding that the CFHR1 and CFHR3 deletion was not polymorphic in the cohort of this study, and none of the SNPs that were significantly associated with AMD in a white population in C2, CFB, and C3 genes showed a significant association with AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.
- NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_assertion evidence source_evidence_literature NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.
- NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_assertion SIO_000772 20523265 NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.
- NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_assertion wasDerivedFrom befree-20150227 NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.
- NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_assertion wasGeneratedBy ECO_0000203 NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP854765.RAcztZLOk7co-3EmfV0AqGk-DBZWYQ7B6je3uuO5OiXtw130_provenance.