Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.
- NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_assertion description "[Mutations in TBX3 that result in reduced functional protein lead to ulnar-mammary syndrome, a developmental disorder characterized by limb, mammary gland, tooth, and genital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.
- NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_assertion evidence source_evidence_literature NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.
- NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_assertion SIO_000772 22535523 NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.
- NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_assertion wasDerivedFrom befree-20140225 NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.
- NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_assertion wasGeneratedBy ECO_0000203 NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP508676.RAON3HfWtnTTythUD7hJpq5G7XofvKO8xDeLrDd4Chhxo130_provenance.