Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.
- NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_assertion description "[Mutations in the NOG gene which encodes the noggin protein, a bone morphogenetic protein antagonist, have been identified in TCS as well as in four other autosomal dominant disorders including proximal symphalangism (SYM1), multiple synostosis (SYNS1), Tarsal-Carpal coalition syndrome and brachydactyly type B (BDB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.
- NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_assertion evidence source_evidence_literature NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.
- NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_assertion SIO_000772 18440889 NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.
- NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_assertion wasDerivedFrom befree-20140225 NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.
- NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_assertion wasGeneratedBy ECO_0000203 NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213107.RAiPAcmpquqiIm7zg9LQFM6ZxCFZmxVm2TFzkHNrtDQxo130_provenance.