Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.
- NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_assertion description "[Familial hemiplegic migraine (FHM) patients do not show hypersensitivity of the calcitonin gene-related peptide (CGRP)-cyclic adenosine 3',5'-monophosphate pathway, as characteristically seen in migraine patients without aura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.
- NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_assertion evidence source_evidence_literature NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.
- NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_assertion SIO_000772 18779512 NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.
- NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_assertion wasDerivedFrom befree-20140225 NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.
- NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_assertion wasGeneratedBy ECO_0000203 NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP752820.RAFh_4nKa2TDlFBpzEzFmPH8taHGgSnKCHVanlV0ISiyw130_provenance.