Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.
- NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_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." NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.
- NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_assertion evidence source_evidence_literature NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.
- NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_assertion SIO_000772 15959366 NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.
- NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_assertion wasDerivedFrom befree-2016 NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.
- NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_assertion wasGeneratedBy ECO_0000203 NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.
- befree-2016 importedOn "2016-02-19" NP499828.RAA0c1om7mtF7rjQ1TlwPzuZ1_qNRoljyRQP7oYGDdaG8130_provenance.