Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.
- NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_assertion description "[Familial hemiplegic migraine (FHM) is genetically heterogeneous with mutations in the CACNA1A (FHM1), ATP1A2 (FHM2) and SCN1A (FHM3) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.
- NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_assertion evidence source_evidence_literature NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.
- NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_assertion SIO_000772 18451712 NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.
- NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_assertion wasDerivedFrom befree-2016 NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.
- NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_assertion wasGeneratedBy ECO_0000203 NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.
- befree-2016 importedOn "2016-02-19" NP669011.RAWmCB5GdtmPO3WSKEYo0q4tOZwSx2EKVpsC5OD6W0gao130_provenance.