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- source_evidence_literature type ECO_0000212 NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.
- NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involve]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.
- NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_assertion evidence source_evidence_literature NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.
- NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_assertion SIO_000772 17903297 NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.
- NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_assertion wasDerivedFrom gad-20150221 NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.
- NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_assertion wasGeneratedBy ECO_0000203 NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.
- gad-20150221 importedOn "2015-02-21" NP112734.RAci3ZCPEuF3VRxLJUMdwfhx3w-U096WXWcZ1OudgUD2Q130_provenance.