Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.
- NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_assertion description "[Genetic defects of the human androgen receptor (AR) can cause a wide spectrum of androgen insensitivity syndromes (AIS) ranging from phenotypic females in those with complete AIS; ambiguous genitalia in partial AIS; to male infertility in minimal AIS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.
- NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_assertion evidence source_evidence_literature NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.
- NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_assertion SIO_000772 9607727 NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.
- NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_assertion wasDerivedFrom befree-20150227 NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.
- NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_assertion wasGeneratedBy ECO_0000203 NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP250583.RAWR6vY3i_Bc32T7act4EqkAk7qZvKcMaLEWXWMXvfhhs130_provenance.