Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.
- NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_assertion description "[Polymorphisms of the ADR gene may alter the untreated IOP level of patients with NTG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.
- NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_assertion evidence source_evidence_literature NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.
- NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_assertion SIO_000772 20705341 NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.
- NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_assertion wasDerivedFrom gad-20130706 NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.
- NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_assertion wasGeneratedBy ECO_0000203 NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.
- gad-20130706 importedOn "2013-07-06" NP88578.RA1m_qp5te86TDLH7FnVV2N5owId-vNfl94SaxsXAvXsc130_provenance.