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- source_evidence_literature type ECO_0000212 NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.
- NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_assertion description "[No significant differences in allele or genotype frequencies for the NOS2A promoter CCTTT repeat microsatellite and NOS3 gene polymorphisms between RA patients with or without CV events were found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.
- NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_assertion evidence source_evidence_literature NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.
- NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_assertion SIO_000772 19327239 NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.
- NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_assertion wasDerivedFrom befree-20140225 NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.
- NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_assertion wasGeneratedBy ECO_0000203 NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP240749.RAr6dIeA6k9tGb_B730sV5jUgeH7vd7LsSpzMxbtr3SSU130_provenance.