Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.
- NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_assertion description "[Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.
- NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_assertion evidence source_evidence_literature NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.
- NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_assertion SIO_000772 15109497 NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.
- NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_assertion wasDerivedFrom befree-2016 NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.
- NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_assertion wasGeneratedBy ECO_0000203 NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.
- befree-2016 importedOn "2016-02-19" NP441501.RAC_KwxiuxRMGc1BrwZanbkbd2oL_kg0ZupOd-JQXt_nE130_provenance.