Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.
- NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_assertion wasGeneratedBy ECO_0000203 NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.
- NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_assertion wasDerivedFrom befree-20140225 NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.
- NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_assertion SIO_000772 20030748 NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.
- NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_assertion evidence source_evidence_literature NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.
- NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_assertion description "[Germline mutations in several members of RAS/RAF/MEK/ERK pathway cause clinically similar genetic disorders, including Noonan syndrome (NS), Costello syndrome (CS) and cardio-facio-cutaneous syndrome (CFC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.
- befree-20140225 importedOn "2014-02-25" NP491008.RAX-tFXFbUH_Oyx9pwQd4rTnFmByH9fHCWV3ims11Fgec130_provenance.