Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_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." NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion evidence source_evidence_literature NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion SIO_000772 18807109 NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion wasDerivedFrom befree-20150227 NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_assertion wasGeneratedBy ECO_0000203 NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP315207.RAEKthq0c8ywieiVjHG4-Mg4kpNU24-OeaeVELNPbPXZI130_provenance.