Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.
- NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_assertion description "[The androgen receptor A645D mutation has been described in one patient with ambiguous genitalia and one boy with normal phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.
- NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_assertion evidence source_evidence_literature NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.
- NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_assertion SIO_000772 16705072 NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.
- NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_assertion wasDerivedFrom befree-20150227 NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.
- NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_assertion wasGeneratedBy ECO_0000203 NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP250588.RAp6sXY1drqsxu0hEkR44nYuLxQSaor06RW3hzrd95Fqg130_provenance.