Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.
- NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_assertion description "[To determine if idiopathic RCM is part of the clinical expression of TNNI3 mutations, genetic investigations of the gene were performed in an additional nine unrelated RCM patients with restrictive filling patterns, bi-atrial dilatation, normal systolic function, and normal wall thickness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.
- NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_assertion evidence source_evidence_literature NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.
- NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_assertion SIO_000772 12531876 NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.
- NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_assertion wasDerivedFrom befree-20150227 NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.
- NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_assertion wasGeneratedBy ECO_0000203 NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP748655.RAp2BiWEgs2zrixzCzBuqNI5i_Ap_QO3IOFbVLmvkiAPs130_provenance.