Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.
- NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_assertion description "[Mutations in the PTEN gene are associated with a broad spectrum of disorders, including Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome, and Lhermitte-Duclos disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.
- NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_assertion evidence source_evidence_curated NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.
- NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_assertion SIO_000772 17427195 NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.
- NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_assertion wasDerivedFrom ctd_human-20150221 NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.
- NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_assertion wasGeneratedBy ECO_0000218 NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP27549.RAuIfy6d7fEtRyOXr_NJH1s_ak-iTp60HniC2sqauBOkw130_provenance.