Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.
- NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_assertion description "[New mutation of the androgen receptor gene, as a deletion in exon 1 not described previously, was identified in a case of complete androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.
- NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_assertion evidence source_evidence_literature NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.
- NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_assertion SIO_000772 18462702 NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.
- NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_assertion wasDerivedFrom lhgdn-20090331 NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.
- NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_assertion wasGeneratedBy ECO_0000203 NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP153399.RA7ANoWm2ty50nR9KwPYjhW8saGmvmXKW-7YRcc1-pikU130_provenance.