Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_assertion> ?p ?o ?g. }
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- NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_assertion type Assertion NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_head.
- NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_assertion description "[A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_provenance.
- NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_assertion evidence source_evidence_curated NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_provenance.
- NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_assertion SIO_000772 9152842 NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_provenance.
- NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_assertion wasDerivedFrom uniprot-20130724 NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_provenance.
- NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_assertion wasGeneratedBy ECO_0000218 NP2266.RArzZtohYHVR1to1GztAL0qYdxgD3-36N0MJp4-Feyt7A130_provenance.