Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.
- NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_assertion description "[The teenage sister of the proband is a carrier of the same LAMP2 mutation and has HCM without skeletal myopathy or WPW.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.
- NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_assertion evidence source_evidence_literature NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.
- NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_assertion SIO_000772 16144992 NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.
- NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_assertion wasDerivedFrom befree-20140225 NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.
- NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_assertion wasGeneratedBy ECO_0000203 NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP660211.RAzRaOEj7GC-kCJwQLu9yMn2-IHB96THNk0X3gRhgxyhE130_provenance.