Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.
- NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_assertion description "[Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: identification of a gene near FRAXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.
- NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_assertion evidence source_evidence_literature NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.
- NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_assertion SIO_000772 7536393 NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.
- NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_assertion wasDerivedFrom befree-20150227 NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.
- NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_assertion wasGeneratedBy ECO_0000203 NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP409164.RA_Mhqr9Gw2-SAwr9Omz4kSeceM0QPxn1XIsthZudUc4c130_provenance.