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- source_evidence_literature type ECO_0000212 NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.
- NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_assertion description "[Neither mutation hot spot nor phenotype?genotype correlation has been established in MEN1 although some missense mutations may be specifically associated with a phenotype of familial isolated hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.
- NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_assertion evidence source_evidence_literature NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.
- NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_assertion SIO_000772 19068082 NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.
- NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_assertion wasDerivedFrom befree-2016 NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.
- NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_assertion wasGeneratedBy ECO_0000203 NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.
- befree-2016 importedOn "2016-02-19" NP708157.RA72UQXIEyB0nP6ACDDvdF3LFWygEEvDrlD37VF-g7NXU130_provenance.