Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_assertion description "[Our data suggest that ChLS is allelic to the ATR-X syndrome with its less severe phenotype being due to the presence of some XNP/ATR-X protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_assertion evidence source_evidence_literature NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_assertion SIO_000772 15508018 NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_assertion wasDerivedFrom befree-20150227 NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_assertion wasGeneratedBy ECO_0000203 NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP257435.RAo-_E04M_BFTmtEK3jSFknKgdQMCtV9IZY1TBw8D_g2k130_provenance.