Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.
- NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_assertion description "[NKX2.5 mutations occur in a small percentage of patients with various congenital heart diseases/. 5 mutations in non-homeodomain regions may be important in the development of human structural cardiac defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.
- NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_assertion evidence source_evidence_literature NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.
- NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_assertion SIO_000772 14607454 NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.
- NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_assertion wasDerivedFrom lhgdn-20090331 NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.
- NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_assertion wasGeneratedBy ECO_0000203 NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP202092.RA3jhRmdpZbZqbT2O3y1WqGXkjxua1Vq4X86Z8nQ-Ld1M130_provenance.