Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance.