Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.
- NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_assertion description "[Two other FGFRs, FGFR1 and FGFR3, also account for craniosynostoses of variable severity [Pfeiffer, Crouzon with acanthosis nigricans (a pre-malignant skin disorder), and Muenke syndromes].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.
- NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_assertion evidence source_evidence_literature NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.
- NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_assertion SIO_000772 14987407 NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.
- NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_assertion wasDerivedFrom befree-20150227 NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.
- NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_assertion wasGeneratedBy ECO_0000203 NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400994.RAQCDZcAdpCKvF3b2JG5bfZOiJxIme36bakMaGsOCsinE130_provenance.