Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.
- NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_assertion description "[Mutations in the lamin A/C gene (LMNA) may cause familial dilated cardiomyopathy (dilated cardiomyopathy) characterized by early onset atrio-ventricular block (A-V block) before the manifestation of dilated cardiomyopathy and high risk of sudden death due to ventricular arrhythmia, which is very similar to the phenotype of gap junction related heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.
- NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_assertion evidence source_evidence_literature NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.
- NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_assertion SIO_000772 20497714 NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.
- NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_assertion wasDerivedFrom befree-20150227 NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.
- NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_assertion wasGeneratedBy ECO_0000203 NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537406.RAUsEla8H8HilM6gbcjAh0NPd-YZ1eywy7KuMd15XyynQ130_provenance.