Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
- NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
- NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_assertion evidence source_evidence_literature NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
- NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_assertion SIO_000772 10442562 NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
- NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_assertion wasDerivedFrom befree-2016 NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
- NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_assertion wasGeneratedBy ECO_0000203 NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.
- befree-2016 importedOn "2016-02-19" NP259989.RAv9NwLwsOIjm0-TXgheM6g_dMOxmUM8MaKZk4DTf668g130_provenance.