Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.
- NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_assertion description "[ZNF261 at Xq13.1 is disrupted by a t(X;13)(q13.1;q32) rearrangement in a mentally retarded patient and is a candidate gene for nonspecific X-linked mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.
- NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_assertion evidence source_evidence_literature NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.
- NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_assertion SIO_000772 10486218 NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.
- NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_assertion wasDerivedFrom befree-20150227 NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.
- NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_assertion wasGeneratedBy ECO_0000203 NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP817432.RAh7QzFvJ0lMCzwGbdmzZWW68weDXIGqvs07BIgd7nblw130_provenance.