Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.
- NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_assertion description "[Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.
- NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_assertion evidence source_evidence_literature NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.
- NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_assertion SIO_000772 11784876 NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.
- NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_assertion wasDerivedFrom befree-20140225 NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.
- NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_assertion wasGeneratedBy ECO_0000203 NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477951.RAXvDdMkjwK_H3fJb2u4O9VPbpRmgNNR4x-PxhJ0kaeSg130_provenance.