Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_assertion> ?p ?o ?g. }
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- NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_assertion type Assertion NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_head.
- NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_assertion wasGeneratedBy ECO_0000203 NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_provenance.
- NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_assertion wasDerivedFrom gad-20150221 NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_provenance.
- NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_assertion SIO_000772 18162506 NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_provenance.
- NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_assertion evidence source_evidence_literature NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_provenance.
- NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_assertion description "[INS mutations are the second most common cause of PND and a rare cause of MODY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116911.RAA4c8DlDLNJytcnkmSHW8BVHuud77BSDdTOzhl9wBBHw130_provenance.