Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_assertion> ?p ?o ?g. }
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- NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_assertion type Assertion NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_head.
- NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_provenance.
- NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_assertion evidence source_evidence_literature NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_provenance.
- NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_assertion SIO_000772 22288654 NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_provenance.
- NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_assertion wasDerivedFrom befree-20140225 NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_provenance.
- NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_assertion wasGeneratedBy ECO_0000203 NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_provenance.