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- source_evidence_literature type ECO_0000212 NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.
- NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_assertion description "[These cases were compared with 370 patients from the French PAH Network (93 with a bone morphogenetic protein receptor type 2 [BMPR2] mutation and 277 considered as idiopathic cases without identified mutation).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.
- NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_assertion evidence source_evidence_literature NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.
- NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_assertion SIO_000772 20056902 NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.
- NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_assertion wasDerivedFrom befree-20140225 NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.
- NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_assertion wasGeneratedBy ECO_0000203 NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP162221.RA-CnGC7CiF5o4_WsTD492dBbA2t7kqFP_LiS8DdK9D3Y130_provenance.