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- source_evidence_literature type ECO_0000212 NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.
- NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_assertion description "[Identification of polymorphic sites within NET, specifically those that produce functional consequences, is one critical step in elucidating the genetic variation contributing to the heritable component of diseases such as ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.
- NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_assertion evidence source_evidence_literature NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.
- NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_assertion SIO_000772 19698724 NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.
- NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_assertion wasDerivedFrom befree-2016 NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.
- NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_assertion wasGeneratedBy ECO_0000203 NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.
- befree-2016 importedOn "2016-02-19" NP758954.RAEE9Won-jKiXigko3Aa1f-U1AqPcaJCipshkxe31kGDg130_provenance.