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- source_evidence_literature type ECO_0000212 NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion evidence source_evidence_literature NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion SIO_000772 18807109 NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion wasDerivedFrom gad-20150221 NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_assertion wasGeneratedBy ECO_0000203 NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP114770.RAf7owZhlQm4aElW5fPXDHKnJ5l2r_m9muaLowKyr66p4130_provenance.