Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion> ?p ?o ?g. }
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- NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion type Assertion NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_head.
- NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion wasGeneratedBy ECO_0000203 NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.
- NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion wasDerivedFrom befree-20140225 NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.
- NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion SIO_000772 21403659 NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.
- NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion evidence source_evidence_literature NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.
- NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion description "[Although some cases of isolated cryptorchidism in humans can be ascribed to known genetic defects, such as mutations in INSL3 or RXFP2, the cause of cryptorchidism remains unknown in most patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.