Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.
- NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_assertion description "[Pfeiffer syndrome (PS) (MIM 101600) is one of the most common syndromic forms of craniosynostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.
- NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_assertion evidence source_evidence_literature NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.
- NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_assertion SIO_000772 23348274 NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.
- NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_assertion wasDerivedFrom befree-20140225 NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.
- NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_assertion wasGeneratedBy ECO_0000203 NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868578.RAod0IWvpi30bL_8FsGGfTuAbPvi6Eszp7kToDpUqp6d8130_provenance.