Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.
- NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_assertion description "[Mutations in FGFR1/FGF8/PROKR2 contributed to 7.8% of our patients with CPHD/SOD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.
- NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_assertion evidence source_evidence_literature NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.
- NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_assertion SIO_000772 22319038 NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.
- NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_assertion wasDerivedFrom befree-2016 NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.
- NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_assertion wasGeneratedBy ECO_0000203 NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_provenance.