Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.
- NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_assertion description "[Horizontal gaze palsy and progressive scoliosis (HGPPS) is an autosomal recessive neurologic disorder caused by homozygous or compound heterozygous mutations in the ROBO3 gene on chromosome 11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.
- NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_assertion evidence source_evidence_literature NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.
- NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_assertion SIO_000772 18829051 NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.
- NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_assertion wasDerivedFrom befree-20140225 NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.
- NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_assertion wasGeneratedBy ECO_0000203 NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP348519.RA44tJWWAkt2yw0UXohXN5hzX2PPwKaKM6_wVow2B8FOg130_provenance.