Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion evidence source_evidence_literature NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion SIO_000772 23768516 NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion wasDerivedFrom befree-20150227 NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion wasGeneratedBy ECO_0000203 NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.