Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.
- NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_assertion description "[Androgen insensitivity syndrome (AIS) is an X-linked genetic disorder of male sexual differentiation caused by mutations in the androgen receptor (AR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.
- NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_assertion evidence source_evidence_literature NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.
- NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_assertion SIO_000772 11587068 NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.
- NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_assertion wasDerivedFrom befree-20140225 NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.
- NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_assertion wasGeneratedBy ECO_0000203 NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP385193.RANfQsXkWwC9trE6vXjSkX24bIRoD6hioZuwrAKUqJnIg130_provenance.