Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.
- NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_assertion description "[We concluded that the NOS1 3'-UTR C276T polymorphism might not play a major role in the susceptibility of TD development, or on the severity of TD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.
- NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_assertion evidence source_evidence_literature NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.
- NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_assertion SIO_000772 15088155 NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.
- NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_assertion wasDerivedFrom befree-20150227 NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.
- NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_assertion wasGeneratedBy ECO_0000203 NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP791918.RAixsYrgEzuDvQqiHMTM2EaxSrS3VHUTHL6urSoidJJWg130_provenance.