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- source_evidence_literature type ECO_0000212 NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.
- NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_assertion description "[Recent molecular studies of the original cases of normokalemic periodic paralysis (normoKPP) have raised suspicions that these families actually had hyperkalemic periodic paralysis (hyperKPP) due to mutations in the skeletal muscle sodium channel gene SCN4A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.
- NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_assertion evidence source_evidence_literature NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.
- NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_assertion SIO_000772 22926674 NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.
- NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_assertion wasDerivedFrom befree-20140225 NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.
- NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_assertion wasGeneratedBy ECO_0000203 NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP271399.RA7RnSATl-Vsd83kEwxv5eIVNFXH9VjL0lkD6-T9BlXFk130_provenance.