Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.
- NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_assertion description "[186 genes showed significant differences in expression following HS (p<0.05), including known HS-inducible genes, as expected, as well as those coding for NGFR and a number of SZ and ASD candidates, including SMARCA2, DPP10, ARNT2, AHI1 and ZNF804A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.
- NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_assertion evidence source_evidence_literature NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.
- NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_assertion SIO_000772 24736721 NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.
- NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_assertion wasDerivedFrom befree-2016 NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.
- NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_assertion wasGeneratedBy ECO_0000203 NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1173823.RAOcJ47knNIeIXWNkrNSIfXRHgDlZTUNGvytlYzEz9CDY130_provenance.