Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_assertion> ?p ?o ?g. }
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- NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_assertion type Assertion NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_head.
- NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_assertion description "[TSP-5 is of interest because mutations in the gene cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED/EDM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_provenance.
- NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_assertion evidence source_evidence_literature NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_provenance.
- NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_assertion SIO_000772 18193163 NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_provenance.
- NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_assertion wasDerivedFrom befree-20140225 NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_provenance.
- NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_assertion wasGeneratedBy ECO_0000203 NP503356.RAQL59hokWECiUBgBkHS8Q0q6UsU5AcimwmIC0BDcbwHY130_provenance.