Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.
- NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_assertion description "[The chromatin-associated protein ATRX was originally identified because mutations in the ATRX gene cause a severe form of syndromal X-linked mental retardation associated with alpha-thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.
- NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_assertion evidence source_evidence_literature NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.
- NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_assertion SIO_000772 17609377 NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.
- NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_assertion wasDerivedFrom befree-20150227 NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.
- NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_assertion wasGeneratedBy ECO_0000203 NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP257579.RAbzY_xHr_s1-PpOgRTZv8WAS5cj24vu1XkDKFU2b91Pg130_provenance.