Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.
- NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_assertion description "[These results reinforce the idea that ARX mutations are relevant to mental retardation and are indicative that molecular screening of exon 2 should be considered in males with mental retardation of unknown etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.
- NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_assertion evidence source_evidence_literature NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.
- NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_assertion SIO_000772 16845484 NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.
- NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_assertion wasDerivedFrom lhgdn-20090331 NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.
- NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_assertion wasGeneratedBy ECO_0000203 NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP190025.RAItGYsP_2O5qvo9uHfmY_JJ0Q-gRv7Ykar0XCwGkLbk0130_provenance.