Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_assertion type Assertion NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_head.
- NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_assertion description "[Identification of a common PEX1 mutation in Zellweger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_provenance.
- NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_assertion evidence source_evidence_curated NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_provenance.
- NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_assertion SIO_000772 10447258 NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_provenance.
- NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_assertion wasDerivedFrom ctd_human-20150221 NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_provenance.
- NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_assertion wasGeneratedBy ECO_0000218 NP25579.RA5VrI1vLGxo6okjHg_JagdHIvXx0ktGrnLstfEcBcAeI130_provenance.