Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.
- befree-2016 importedOn "2016-02-19" NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.
- NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_assertion wasGeneratedBy ECO_0000203 NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.
- NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_assertion wasDerivedFrom befree-2016 NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.
- NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_assertion SIO_000772 20082464 NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.
- NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_assertion evidence source_evidence_literature NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.
- NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_assertion description "[These observations suggest that some individuals with FBN1 mutations have significant aortic disease involvement of other systems that is typical of FBN1 mutation-related syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787808.RARCw8cFT01PEBBOscTw2z4Ns2cIJ7iQjaUgkbJc18Ve8130_provenance.