Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.
- NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_assertion description "[Mutations in exon 11 of MEF2A gene exist in the patients with CAD, and the mutations may be pathological.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.
- NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_assertion evidence source_evidence_literature NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.
- NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_assertion SIO_000772 16767660 NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.
- NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_assertion wasDerivedFrom gad-20130706 NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.
- NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_assertion wasGeneratedBy ECO_0000203 NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP65674.RADbYQu0T7xnlHTTDefQWD9uxJldiXgi-mH54d8_wwodE130_provenance.