Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.
- befree-2016 importedOn "2016-02-19" NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.
- NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_assertion wasGeneratedBy ECO_0000203 NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.
- NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_assertion wasDerivedFrom befree-2016 NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.
- NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_assertion SIO_000772 21594993 NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.
- NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_assertion evidence source_evidence_literature NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.
- NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_assertion description "[This phenotype which is different from that of classical Marfan syndrome could be caused by a truncated FBN1 protein which could escape nonsense-mediated RNA decay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895337.RACXGUnWVcB57z1Ni87eqQl7ukeo9tJ7QdJorit_XDCGc130_provenance.