Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.
- NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_assertion description "[Besides identifying 8 SCN5A mutations in the present cohort, a KCNE3 T4A mutation was found in a 55-year-old male patient who had experienced several episodes of syncope.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.
- NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_assertion evidence source_evidence_literature NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.
- NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_assertion SIO_000772 22987075 NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.
- NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_assertion wasDerivedFrom befree-2016 NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.
- NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_assertion wasGeneratedBy ECO_0000203 NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1013706.RAU3KSsoFapy_L11bIrou2OvBxpWJR-BC4N8Q_N9t5Dsw130_provenance.