Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_assertion evidence source_evidence_literature NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_assertion SIO_000772 10554356 NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_assertion wasDerivedFrom befree-20150227 NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_assertion wasGeneratedBy ECO_0000203 NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.