Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.
- NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_assertion description "[Any variant that affects CaM expression and/or function may impact on FHC clinical expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.
- NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_assertion evidence source_evidence_literature NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.
- NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_assertion SIO_000772 19429631 NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.
- NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_assertion wasDerivedFrom befree-20140225 NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.
- NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_assertion wasGeneratedBy ECO_0000203 NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP792891.RAVMN9CBtfYJrgZVedE5GnlHxoGMAOaMkUsrtq_Q6HPBs130_provenance.