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- source_evidence_literature type ECO_0000212 NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.
- NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_assertion description "[While non-malformation phenotypes tend to be caused by pathogenic variations that are predicted to expand the first two polyalanine tracts of ARX, or alter residues outside of the homeodomain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.
- NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_assertion evidence source_evidence_literature NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.
- NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_assertion SIO_000772 19507262 NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.
- NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_assertion wasDerivedFrom befree-20150227 NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.
- NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_assertion wasGeneratedBy ECO_0000203 NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835462.RAQXQB1hron0ROvf75JkDQ9m0glRNJQ1J6a09xWcvlCxs130_provenance.