Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.
- NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_assertion wasGeneratedBy ECO_0000203 NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.
- NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_assertion wasDerivedFrom befree-20140225 NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.
- NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_assertion SIO_000772 16791849 NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.
- NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_assertion evidence source_evidence_literature NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.
- NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_assertion description "[In order to be able to find the mutation that is indeed responsible for a MFS-related phenotype, we also propose that genetic testing for sequence alterations in TGFBR1 and TGFBR2 should be complemented by mutation screening of the FBN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP311072.RAnPlURGulFUgY5rD_MBrDGq6XkLoqaGDGmn_vqSPNVZ4130_provenance.