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- source_evidence_literature type ECO_0000212 NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.
- NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_assertion description "[The association was confirmed in an independent CAD case-control sample (CATHGEN) and strong association with MI was identified with single nucleotide polymorphisms (SNPs) in the 3' end of FAM5C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.
- NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_assertion evidence source_evidence_literature NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.
- NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_assertion SIO_000772 18430236 NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.
- NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_assertion wasDerivedFrom befree-20140225 NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.
- NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_assertion wasGeneratedBy ECO_0000203 NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP926647.RAEApcWm_0XhjY5y7sNnr6VLKxLg9ZcRIjtdGpNAm27lQ130_provenance.