Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.
- NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_assertion description "[Recent reports have implicated mutations in the transcription factor NKX2.5 as a cause of various congenital heart defects (CHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.
- NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_assertion evidence source_evidence_literature NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.
- NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_assertion SIO_000772 14607454 NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.
- NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_assertion wasDerivedFrom befree-2016 NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.
- NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_assertion wasGeneratedBy ECO_0000203 NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.
- befree-2016 importedOn "2016-02-19" NP419881.RA7u8Qp7GeYpbmOOxoC_BznNKHnZmPG7ieIZFOGU23LhU130_provenance.