Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.
- NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_assertion description "[We have used pulsed-field gel electrophoresis to study the short arm of the Y chromosome by using a pseudoautosomal probe (MIC2Y) and adjacent Y-specific sequences 27a and 47z (DSXY5) in XX males and XY females, in order to detect chromosomal breakpoints which may have given rise to these individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.
- NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_assertion evidence source_evidence_literature NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.
- NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_assertion SIO_000772 2705458 NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.
- NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_assertion wasDerivedFrom befree-20140225 NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.
- NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_assertion wasGeneratedBy ECO_0000203 NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP593700.RAhP30bjtekbMQ9Pzyj5dtIXKogtRyakLhXN-j6XrxA0Y130_provenance.