Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.
- befree-2016 importedOn "2016-02-19" NP521180.RA9xjEmS0TJEk8Gftxr06wxFbXh9ILHZ1-FKvsew1u1zo130_provenance.
- 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.