Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.
- NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_assertion description "[Familial isolated primary hyperparathyroidism is a distinct genetic variant of the MEN1 syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.
- NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_assertion evidence source_evidence_literature NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.
- NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_assertion SIO_000772 18084346 NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.
- NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_assertion wasDerivedFrom lhgdn-20090331 NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.
- NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_assertion wasGeneratedBy ECO_0000203 NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP130810.RAnpJhpKM7qeuwTBBm-RPwO7A0QP1rS1rvxE_LV0m6i6Q130_provenance.