Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.
- NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_assertion description "[These findings demonstrate the involvement of FGF3 mutations in a human malformation syndrome for the first time and contribute to our understanding of the role this gene plays in embryonic development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.
- NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_assertion evidence source_evidence_literature NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.
- NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_assertion SIO_000772 17236138 NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.
- NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_assertion wasDerivedFrom befree-20140225 NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.
- NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_assertion wasGeneratedBy ECO_0000203 NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP555703.RAT6-aW1awDcPPoGY_PYWwMi0SVOFvHGewfc_FCTXt-Nk130_provenance.