Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_assertion evidence source_evidence_literature NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_assertion SIO_000772 19206178 NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_assertion wasDerivedFrom befree-20140225 NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_assertion wasGeneratedBy ECO_0000203 NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP568483.RA-WGjJ80onUSeVM-A1pt21iE2Kv3A9pTiisUQsX-6rMg130_provenance.