Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.
- NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_assertion description "[A unique point mutation in the androgen receptor gene in a family with complete androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.
- NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_assertion evidence source_evidence_literature NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.
- NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_assertion SIO_000772 1426313 NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.
- NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_assertion wasDerivedFrom befree-2016 NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.
- NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_assertion wasGeneratedBy ECO_0000203 NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.
- befree-2016 importedOn "2016-02-19" NP413405.RAf7a7p3M3rnHhh8xccfaxLWeXzl7HPtVNWIG7-QpRyOs130_provenance.