Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.
- NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_assertion description "[X-linked lissencephaly with corpus callosum agenesis and ambiguous genitalia in genotypic males is associated with mutations of the ARX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.
- NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_assertion evidence source_evidence_literature NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.
- NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_assertion SIO_000772 15921228 NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.
- NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_assertion wasDerivedFrom befree-20140225 NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.
- NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_assertion wasGeneratedBy ECO_0000203 NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.
- befree-20140225 importedOn "2014-02-25" NP852007.RAImGXDI4d9qrlygvMnaBIBf7JVHdSisYDVrPrj_aS5to130_provenance.