Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.
- NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_assertion description "[We directly sequenced the full coding and flanking splice-junctional regions of the HRPT2 gene in 21 parathyroid carcinomas from 15 patients who had no known family history of primary hyperparathyroidism or the HPT-JT syndrome at presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.
- NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_assertion evidence source_evidence_literature NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.
- NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_assertion SIO_000772 14585940 NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.
- NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_assertion wasDerivedFrom befree-20140225 NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.
- NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_assertion wasGeneratedBy ECO_0000203 NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP601471.RAxRFwhhN6sH_IEZoi3ozghNwf9dzqcIK3Ap0Qk9_8R3s130_provenance.