Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.
- NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_assertion description "[Phenotypic variability was observed among patients with the same mutations, particularly the presence and age of onset of hypocortisolism, the levels of PRL and the results of pituitary imaging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.
- NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_assertion evidence source_evidence_literature NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.
- NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_assertion SIO_000772 16984240 NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.
- NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_assertion wasDerivedFrom befree-20150227 NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.
- NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_assertion wasGeneratedBy ECO_0000203 NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP646713.RAkBv1Vbn1rqqdHtgQgZWaLR22t2mRRiUw2HyoEXxhv7g130_provenance.