Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.
- NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_assertion wasGeneratedBy ECO_0000203 NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.
- NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_assertion wasDerivedFrom befree-20140225 NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.
- NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_assertion SIO_000772 19073947 NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.
- NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_assertion evidence source_evidence_literature NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.
- NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_assertion description "[Mutations in FLNA (Xq28) and ARFGEF2 (20q13) are responsible for X-linked bilateral PH and a rare autosomal recessive form of PH with microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476686.RAMQDk3Qx_BUFos6WrG5GG5Wo9F7bcLU14mS3clfp9TUQ130_provenance.