Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.
- NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_assertion description "[This study suggests a mechanism for the generation of different neuropsychiatric symptoms in AD from a single nucleotide polymorphism with reduced receptor binding in T102C 5-HT2A receptor gene homozygotes correlating with susceptibility to depressive symptoms, whereas the relative preservation of receptor binding in heterozygotes with AD correlating with susceptibility to hallucinations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.
- NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_assertion evidence source_evidence_literature NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.
- NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_assertion SIO_000772 17481814 NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.
- NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_assertion wasDerivedFrom befree-20140225 NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.
- NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_assertion wasGeneratedBy ECO_0000203 NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.
- befree-20140225 importedOn "2014-02-25" NP381893.RAq7o0QUEVsH1ega3gOSC7-poKWp0_g8QpUaTg0uD73ak130_provenance.