Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.
- NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_assertion description "[We concluded that AGT and AT1 polymorphisms are independent genetic risk factors for lacunar infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.
- NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_assertion evidence source_evidence_literature NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.
- NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_assertion SIO_000772 10701810 NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.
- NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_assertion wasDerivedFrom befree-2016 NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.
- NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_assertion wasGeneratedBy ECO_0000203 NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.
- befree-2016 importedOn "2016-02-19" NP277025.RAycK2xEuvQ3Sm01vbgL31AqqRQ1VPh3PcC3VHzr6vLT4130_provenance.