Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.
- NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_assertion description "[Therefore, the authors' data provide supportive evidence that mutations in the coding region of the NKX2-5 gene and sequence variants within its promoter region may be among the contributors to the CHD etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.
- NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_assertion evidence source_evidence_literature NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.
- NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_assertion SIO_000772 22576768 NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.
- NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_assertion wasDerivedFrom befree-20150227 NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.
- NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_assertion wasGeneratedBy ECO_0000203 NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333986.RAGLPwQjV8KID2XMbdKxLsn7QgSJ2NbIbarOno6jQHeAk130_provenance.