Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.
- NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_assertion description "[However, unlike the Apert syndrome Pro253Arg FGFR2c mutant, neither the Pfeiffer syndrome Pro250Arg FGFR1c mutant nor the Muenke syndrome Pro250Arg FGFR3c mutant bound appreciably to FGF7 or FGF10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.
- NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_assertion evidence source_evidence_literature NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.
- NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_assertion SIO_000772 14613973 NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.
- NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_assertion wasDerivedFrom befree-20150227 NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.
- NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_assertion wasGeneratedBy ECO_0000203 NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.
- befree-20150227 importedOn "2015-02-27" NP401070.RAQmQ-pEoRXjPXqE1auh8x6UDZBJNtQuflOP4rxdMAdww130_provenance.