Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.
- NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_assertion wasGeneratedBy ECO_0000203 NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.
- NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_assertion wasDerivedFrom befree-20150227 NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.
- NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_assertion SIO_000772 21403659 NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.
- NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_assertion evidence source_evidence_literature NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.
- NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_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." NP513442.RAdfF3GQZmQIIDRkXhx2G1OeO2nP0ESHQumbhxRylVCtw130_provenance.