Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.
- NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_assertion description "[TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.
- NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_assertion evidence source_evidence_literature NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.
- NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_assertion SIO_000772 19068278 NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.
- NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_assertion wasDerivedFrom befree-20150227 NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.
- NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_assertion wasGeneratedBy ECO_0000203 NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP724208.RAxbMSaj0cRaSQ2a87KG1iDr4-cLx5ccBgIMgQRkoI-NY130_provenance.