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- source_evidence_literature type ECO_0000212 NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_assertion evidence source_evidence_literature NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_assertion SIO_000772 19412328 NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_assertion wasDerivedFrom gad-20150221 NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_assertion wasGeneratedBy ECO_0000203 NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.