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- NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_assertion type Assertion NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_head.
- NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_assertion wasGeneratedBy ECO_0000203 NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.
- NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_assertion wasDerivedFrom befree-2016 NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.
- NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_assertion SIO_000772 16272056 NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.
- NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_assertion evidence source_evidence_literature NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.
- NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_assertion description "[Aiming towards an understanding of the molecular background of retinitis pigmentosa, this paper describes the phenotype of a Swedish family with a mutation in IMPDH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.