Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.
- NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_assertion description "[The results presented indicate that mutations in the coding sequences, in the intron-exon boundaries and in the main regulatory regions of the GRIK1 are not commonly involved in the etiology of JAE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.
- NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_assertion evidence source_evidence_literature NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.
- NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_assertion SIO_000772 11920863 NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.
- NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_assertion wasDerivedFrom befree-20140225 NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.
- NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_assertion wasGeneratedBy ECO_0000203 NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP292175.RADjiFt8_-3OLcEN6xwZME3XaKfv_QbRfG4AgEejZqVrU130_provenance.