Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.
- NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_assertion description "[TSP-5 is of interest because mutations in the gene cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED/EDM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.
- NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_assertion evidence source_evidence_literature NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.
- NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_assertion SIO_000772 18193163 NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.
- NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_assertion wasDerivedFrom befree-20150227 NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.
- NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_assertion wasGeneratedBy ECO_0000203 NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320602.RAjUeIl1wnjXbiArotlIuPmUyQYni8mIvR343rk7TySRs130_provenance.