Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.
- NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_assertion description "[X-linked lissencephaly with abnormal genitalia (XLAG) is a rare disorder caused by mutations in the aristaless-related homeobox (ARX) gene, located on Xp22.13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.
- NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_assertion evidence source_evidence_literature NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.
- NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_assertion SIO_000772 18458920 NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.
- NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_assertion wasDerivedFrom befree-20140225 NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.
- NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_assertion wasGeneratedBy ECO_0000203 NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP353015.RAsYOStStmlJYA0I4F1TQMhz_EuGklGSTXKGSGnqxljqs130_provenance.