Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.
- NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_assertion description "[GPC1 and/or STK25 haploinsufficiency may also contribute to the AHO-like phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.
- NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_assertion evidence source_evidence_literature NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.
- NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_assertion SIO_000772 15521982 NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.
- NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_assertion wasDerivedFrom befree-2016 NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.
- NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_assertion wasGeneratedBy ECO_0000203 NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.
- befree-2016 importedOn "2016-02-19" NP467156.RAtG4Mc8upFaill51gnS8X4450AjbCIHFNcXspe5wq1PI130_provenance.