Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.
- NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_assertion description "[Our data extend the number of SNPs present in the promoter region that could play a regulatory role in COMT gene and suggest that the genetic polymorphisms rs 165656 and rs 4646310 exert a role in TMD susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.
- NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_assertion evidence source_evidence_literature NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.
- NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_assertion SIO_000772 23446089 NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.
- NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_assertion wasDerivedFrom befree-20150227 NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.
- NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_assertion wasGeneratedBy ECO_0000203 NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP321790.RAcYaZKdYxNg3UIbVdBDvV4AUQsvni23Ia1RC13HR8USw130_provenance.