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- source_evidence_literature type ECO_0000212 NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.
- NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_assertion description "[We identified mutations of the SH2D1A gene only in the majority of patients presenting with fatal mononucleosis or an XLP family history, but not in any of the other patients studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.
- NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_assertion evidence source_evidence_literature NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.
- NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_assertion SIO_000772 12224001 NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.
- NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_assertion wasDerivedFrom befree-2016 NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.
- NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_assertion wasGeneratedBy ECO_0000203 NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.
- befree-2016 importedOn "2016-02-19" NP367616.RALRKO2LbfVr0v2iQco11heU0Ja_jGNnmjxfflDAwt88g130_provenance.