Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_assertion> ?p ?o ?g. }
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- NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_assertion type Assertion NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_head.
- NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_assertion description "[The clinical and genetic aspects of these families confirm that this syndrome can be clinically variable, with different mutations in the FGFR2 responsible for PS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_provenance.
- NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_assertion evidence source_evidence_literature NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_provenance.
- NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_assertion SIO_000772 25129254 NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_provenance.
- NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_assertion wasDerivedFrom befree-2016 NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_provenance.
- NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_assertion wasGeneratedBy ECO_0000203 NP1211266.RA7MJO_HtBj3YDk6Je3VAAwEzMiHWypB2ntYNMNdkc4LU130_provenance.