Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.
- NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_assertion description "[Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.
- NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_assertion evidence source_evidence_literature NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.
- NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_assertion SIO_000772 16958040 NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.
- NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_assertion wasDerivedFrom befree-20150227 NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.
- NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_assertion wasGeneratedBy ECO_0000203 NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.
- befree-20150227 importedOn "2015-02-27" NP885760.RAlA6PWmGAWZ2-Nii-peU2w2Yms1osyHBwRR6L85Vq778130_provenance.