Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_assertion> ?p ?o ?g. }
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- NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_assertion type Assertion NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_head.
- NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_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." NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_provenance.
- NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_assertion evidence source_evidence_literature NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_provenance.
- NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_assertion SIO_000772 10442562 NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_provenance.
- NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_assertion wasDerivedFrom befree-20140225 NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_provenance.
- NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_assertion wasGeneratedBy ECO_0000203 NP862574.RAPNDYTmuqm9-gKK-NRjR7Dd3dbfvkfhhryVz0silVX7A130_provenance.