Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_assertion> ?p ?o ?g. }
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- NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_assertion type Assertion NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_head.
- NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_assertion description "[Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_provenance.
- NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_assertion evidence source_evidence_literature NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_provenance.
- NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_assertion SIO_000772 11487566 NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_provenance.
- NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_assertion wasDerivedFrom befree-20140225 NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_provenance.
- NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_assertion wasGeneratedBy ECO_0000203 NP158992.RAdU2pO8GPMEX8m5za8wF_GXOmUK6cnp4t3a08b7oR91E130_provenance.