Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion evidence source_evidence_literature NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion SIO_000772 17221017 NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion wasDerivedFrom befree-20140225 NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion wasGeneratedBy ECO_0000203 NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.