Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.
- NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_assertion description "[While the noggin gene (NOG) is not mutated in patients who have FOP, these findings extend a growing body of evidence implicating overactivity of the BMP signaling pathway in the molecular pathogenesis of FOP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.
- NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_assertion evidence source_evidence_literature NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.
- NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_assertion SIO_000772 15959366 NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.
- NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_assertion wasDerivedFrom befree-20150227 NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.
- NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_assertion wasGeneratedBy ECO_0000203 NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP818656.RAWR6qKe0PKC3_kQlmSa6QeDt4TKCj68ZA8DuBJDGFg5k130_provenance.