Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.
- NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_assertion description "[Mutations in chromosome X open reading frame 6 (CXorf6), a recently described candidate gene involved in the development of male genitalia, have been found in patients with complex 46,XY disorders of sexual development (46,XY DSD) including micropenis, bifid scrotum, and penoscrotal hypospadias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.
- NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_assertion evidence source_evidence_literature NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.
- NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_assertion SIO_000772 18635673 NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.
- NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_assertion wasDerivedFrom befree-20150227 NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.
- NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_assertion wasGeneratedBy ECO_0000203 NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835376.RAVWNxp3dVcOr9wDhPQckld1RWzdH_hYpq6nYT6f-VJfA130_provenance.