Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_assertion> ?p ?o ?g. }
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- NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_assertion type Assertion NP959591.RAkekrL6y1uXpIWdnDFPXN06o5psrC3ELJOvlXTpDvBKw130_head.
- 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.