Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.
- NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_assertion description "[The second phenotype, observed in four unrelated families, is autosomal dominant trismus-pseudocamptodactyly syndrome (distal arthrogryposis type 7; previously associated exclusively with myosin heavy chain 8 mutations).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.
- NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_assertion evidence source_evidence_literature NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.
- NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_assertion SIO_000772 23413262 NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.
- NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_assertion wasDerivedFrom befree-20150227 NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.
- NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_assertion wasGeneratedBy ECO_0000203 NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583448.RA38dOlSfB4_wYOcmIdxJiybpmAdYTAhsSSjF_WVjB65E130_provenance.