Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.
- NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_assertion description "[Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.
- NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_assertion evidence source_evidence_literature NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.
- NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_assertion SIO_000772 18467358 NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.
- NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_assertion wasDerivedFrom befree-2016 NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.
- NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_assertion wasGeneratedBy ECO_0000203 NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP670056.RAx20S2Cc5JNytGM9qau3oj695ODpOz-_F3FYmG5EtyYQ130_provenance.