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- source_evidence_literature type ECO_0000212 NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.
- NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_assertion description "[As in previously studied patients, adFNDI apparently manifested after birth, was due to a partial or severe deficiency of AVP, and was associated with absence or diminution of the hyperintense MRI signal normally emitted by the posterior pituitary, and with a heterozygous mutation in the AVP-NPII gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.
- NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_assertion evidence source_evidence_literature NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.
- NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_assertion SIO_000772 11980620 NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.
- NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_assertion wasDerivedFrom befree-20150227 NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.
- NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_assertion wasGeneratedBy ECO_0000203 NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP964653.RAjQEhsx9I_0eusYF6LPPm5kdYLk7X9I6nYy80WFRYIaQ130_provenance.