Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.
- NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_assertion description "[We did not find a mutation in either multi-minicore disease-associated gene, SEPN1, or major distal myopathy-related genes, including GNE, ZASP, MYOT, exons 32-36 of MYH7, and the last exon of TTN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.
- NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_assertion evidence source_evidence_literature NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.
- NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_assertion SIO_000772 19797833 NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.
- NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_assertion wasDerivedFrom befree-20140225 NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.
- NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_assertion wasGeneratedBy ECO_0000203 NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP444349.RAi9iId12JWISo5a34ObJ4y-rpBNTtlqr5dcLWB0-2JGM130_provenance.